REPORT OF THE RESUMED SESSION OF THE EXTRAORDINARY
MEETING OF THE CONFERENCE OF THE PARTIES FOR THE ADOPTION OF THE
PROTOCOL ON BIOSAFETY TO THE CONVENTION ON BIOLOGICAL DIVERSITY:
24-28 JANUARY 2000
The Convention on Biological Diversity (CBD), negotiated under the
auspices of the United Nations Environment Programme (UNEP), was
adopted on 22 May 1992 and entered into force on 29 December 1993.
There are currently 176 Parties to the Convention. Article 19.3 of the
CBD provides for Parties to consider the need for and modalities of a
protocol setting out procedures in the field of the safe transfer,
handling and use of living modified organisms (LMOs) that may have an
adverse effect on biodiversity and its components.
COP-1: The first Conference of the Parties (COP-1) to the CBD, held
in Nassau, the Bahamas, from 28 November - 9 December 1994,
established an Open-ended Ad Hoc Group of Experts on Biosafety,
which met in Madrid from 24-28 July 1995. According to this meeting's
report (UNEP/CBD/COP.2/7), most delegations favored the development of
an international framework on biosafety under the CBD. Elements
favored unanimously for such a framework included: all activities
related to LMOs that may have adverse effects on biodiversity;
transboundary movement of LMOs; release of LMOs in centers of
origin/genetic diversity; mechanisms for risk assessment and
management; procedures for advance informed agreement (AIA);
information exchange; capacity-building and implementation; and
definition of terms. Elements with partial support included:
socio-economic considerations; liability and compensation; and
financial issues.
COP-2: At COP-2 in Jakarta, Indonesia, in November 1995, delegates
considered the need for and modalities of a protocol on biosafety.
Amidst debate over the Protocol's scope, the COP adopted compromise
language (Decision II/5) calling for a "negotiation process to
develop in the field of the safe transfer, handling and use of living
modified organisms, a protocol on biosafety, specifically focusing on
transboundary movement of any LMO that may have an adverse effect on
biological diversity." COP-2 also established an Open-ended Ad
Hoc Working Group on Biosafety (BSWG) to elaborate a protocol
based on elements from the Madrid report. Other terms of reference for
the BSWG state that it shall: elaborate key terms and concepts;
consider AIA procedures; identify relevant categories of LMOs; and
develop a protocol that takes into account the precautionary principle
and requires Parties to establish national measures.
BSWG-1: At its first meeting, held in Aarhus, Denmark, from 22-26
July 1996, the BSWG elected Veit Koester (Denmark) as its Chair and
began the elaboration of a protocol on biosafety. Although the meeting
produced few written results, it functioned as a forum for defining
issues and articulating positions characteristic of a pre-negotiation
process. Governments listed elements for a future protocol and
outlined the information required to guide their future work.
BSWG-2: Delegates to BSWG-2, held from 12-16 May 1997, in Montreal,
discussed a range of issues, including: objectives; AIA; notification
procedures for transfers of LMOs; national competent authorities/focal
points; information-sharing and a clearing-house mechanism;
capacity-building; public participation and awareness; risk assessment
and management; unintentional transboundary movement; handling,
transportation, packaging and transit requirements; and monitoring and
compliance. BSWG-2 also convened a contact group to start defining key
terms.
BSWG-3: BSWG-3 met in Montreal from 13-17 October 1997. Delegates
produced a consolidated draft text to serve as the basis for
negotiation. The meeting established two Sub-Working Groups to address
the core articles of the Protocol, as well as a contact group on
institutional matters and final clauses. Delegates addressed
outstanding issues in plenary, including: socio-economic
considerations; liability and compensation; illegal traffic;
non-discrimination; trade with non-Parties; as well as objectives,
general obligations, title and preamble for a protocol.
BSWG-4: At the opening of BSWG-4, which met in Montreal from 5-13
February 1998, delegates entered the "negotiation phase" in
order to reduce, through consensus, the number of options under each
article. Using the structure adopted at BSWG-3, delegates began
consideration of several articles that had only received preliminary
discussion at BSWG-3, including: principles/objectives, general
obligations, non-discrimination, socio-economic considerations, and
liability and compensation. Delegates also continued work on other
issues previously addressed, including: matters relating to AIA, risk
assessment and management, minimum national standards, emergency
measures and capacity-building.
COP-4: The Fourth Meeting of the Conference of the Parties (COP- 4)
to the CBD took place from 4-15 May 1998, in Bratislava, Slovakia. In
Decision IV/3, "Issues related to biosafety," the COP
extended the deadline for the negotiation of a protocol from the end
of 1998 to early 1999. It established an extra meeting to be followed
by an ExCOP to adopt the Protocol in 1999.
BSWG-5: BSWG-5 met from 17-28 August 1998, in Montreal. Delegates
consolidated options for 45 articles in the revised consolidated draft
to 40 articles, although thirteen articles remained entirely
bracketed. Polarized positions continued to emerge during discussions
over whether the Protocol's scope included "products
thereof," whether the Protocol would address questions of
liability and redress, and if the Protocol would incorporate the
precautionary principle.
BSWG-6 & EXCOP: BSWG-6 met from 14-22 February 1999, and was
immediately followed by the First Extraordinary Meeting of the
Conference of the Parties, held from 22-23 February 1999, in Cartagena
de Indias, Colombia. Despite intense negotiations, delegates were not
able to agree on a protocol, although identifiable negotiating groups
started to emerge. The main areas of contention centered on trade
issues, treatment of commodities and domestic vs. international
regulatory regimes. The ExCOP adopted a decision to suspend the
meeting and requested the ExCOP President and the COP-4 Bureau to
decide when and where the session would resume, no later than the
fifth meeting of the Conference of the Parties. Delegates decided that
the Protocol will be called the Cartagena Protocol on Biosafety to the
CBD. The text of the draft Protocol, set out in both the Report of
BSWG-6 and the ExCOP Draft Report (UNEP/CBD/ExCOP/1/L.2/ Rev.1), was
transmitted to the resumed ExCOP session for further debate.
INFORMAL CONSULTATIONS: Three sets of informal consultations aimed
at facilitating discussion on key outstanding issues were held during
the period between the ExCOP’s suspension and its resumption. (Note:
Since the third set of consultations immediately preceding the resumed
ExCOP, its report has been merged with the report of the ExCOP below.)
Montreal (July 1999): Based on a decision by the COP-4 Bureau, on 1
July 1999, ExCOP President Mayr met with spokespersons from the major
negotiating groups that emerged in Cartagena: the Central and Eastern
European countries, the Compromise Group (Japan, Mexico, Norway, South
Korea and Switzerland), the European Union (EU), the Like-Minded Group
(the majority of developing countries) and the Miami Group (Argentina,
Australia, Canada, Chile, the United States and Uruguay). At the
meeting, the groups expressed their political will to finalize
negotiations and it was agreed to hold another set of informal
consultations prior to resuming the ExCOP.
Vienna (September 1999): The second set of informal consultations
met in Vienna, Austria, from 15-19 September 1999. The first two days
of the meeting were devoted to consultations within negotiating
groups; the third day was for informal exchanges between groups; and
the final two days were devoted to resolving differences between
groups on pending core issues. During the final two days of
discussions, chaired by ExCOP President Mayr, negotiating groups met
in the "Vienna setting," a roundtable format with two
spokespersons from each group. The groups addressed the issues of
commodities, the protocol's relationship with other international
agreements, the protocol's scope and application of the AIA procedure.
Negotiating groups agreed on a basic set of concepts for commodities
and relations with other international agreements, while acknowledging
that the central differences on those and other issues remain. The
results were forwarded as a Chairman’s Summary (UNEP/CBD/ExCOP/1/INF/3)
to the resumed session of the ExCOP.
The third set of informal consultations were held in Montreal from
20-23 January 2000. The first two days of the informal consultations
were devoted to discussions within negotiating groups and were chaired
by ExCOP President Juan Mayr. On Saturday, 22 January, Chair Mayr
opened informal discussions among the major negotiating groups in the
"Vienna setting." Chair Mayr highlighted his non-paper,
which provided suggested text incorporating the results of the Vienna
discussions on scope, application of the AIA as it relates to
commodities, and Article 31 (Relationship with Other International
Agreements) of the draft Protocol contained in the ExCOP Draft Report.
The negotiating groups provided opening remarks in which they
reiterated their political will to conclude the Protocol.
After providing initial comments on the non-paper, Chair Mayr
proposed that consultations proceed by clustering related issues into
three groups. The first being commodities, including a new article in
Chair Mayr’s non-paper on an alternative AIA for living modified
organisms intended for direct use for food or feed, or for processing
(LMO-FFPs), as well as articles in the ExCOP Draft Report on: the
application of the AIA procedure; handling, transport, packaging and
identification; information-sharing and the biosafety clearing-house;
and a new annex in the non-paper on information requirements for
notifications. The second cluster was on scope, covering Article 4 of
the ExCOP Draft Report. The final cluster included the Protocol’s
relationship with other international agreements, as well as articles
from the ExCOP Draft Report on: Parties’ rights to take more
protective measures than those in the Protocol; the precautionary
principle; non-discrimination; and socio-economic considerations. On
the third cluster, the EU supported the formulation, but indicated
that discussion of other issues should not be reopened. The
Like-Minded Group requested removal of discussion on Parties’ rights
to take more protective measures than those in the protocol, the
precautionary principle, and socio-economic considerations, while the
Miami Group argued to retain them.
The negotiating groups provided initial comments on the commodities
and scope clusters, which were then discussed by contact groups on
Sunday, 23 January. The "Vienna setting" convened to hear
the contact groups’ progress reports. After closing comments by the
groups in the evening "Vienna setting," Chair Mayr indicated
that he would forward the results to Monday’s resumed ExCOP and
closed the informal session.
RESUMED EXCOP
Editors’ Note: Respecting the confidential nature of informal
consultations and contact group meetings, the Bulletin does not
use the names of countries and/or groups in its reports of these
meetings.
On Monday, 24 January 2000, COP-4 President Laszlo Miklös
(Slovakia) welcomed delegates on behalf of the COP-4 Bureau. ExCOP
President Juan Mayr officially opened the ExCOP for the Adoption of
the Protocol on Biosafety, inviting delegates to build on the work
accomplished during the recent informal consultations. He stressed the
urgency to build on this momentum to solve outstanding issues and to
adopt the protocol as the first international environmental treaty of
the new millennium. He encouraged Ministers to attend and drew
attention to a ministerial dinner roundtable he would host on
Wednesday.
CBD Executive Secretary Hamdallah Zedan emphasized the significance
of the negotiations for the CBD and sustainable development. He
referred to the benefits of biotechnology and said the protocol would
ensure that humanity enjoys the benefits of science and trade, while
protecting the environment. He noted the atmosphere of cautious
optimism apparent during the informal consultations and expressed
appreciation to Parties that provided financial support for the
participation of developing countries and those with economies in
transition.
Delegates then adopted the provisional revised agenda (UNEP/ CBD/ExCOP/1/1/Rev.2)
and its annotations (UNEP/CBD/ExCOP/1/ 1/Rev.2/Add.1). Regarding the
organization of work, Mayr said that the Plenary and the "Vienna
setting" involving groups’ spokespersons would be used and both
would have translation and follow official rules of procedure. He also
stated that there would not be more than two contact groups meeting in
parallel. Mayr proposed keeping the contact groups on scope and
commodities, which were established during the recent informal
consultations. Ethiopia, on behalf of the Like-Minded Group, suggested
that the contact groups be merged. Mayr invited regional groups to
submit names of three representatives for the Legal Drafting Group to
be chaired by Lynn Holowesko (the Bahamas). Participants heard reports
from the CBD Secretariat on the credentials of representatives and on
available documents, including the Draft Report of the First ExCOP (UNEP/CBD/ExCOP/1/L.2/
Rev.1) and the Report of the Sixth Open-ended Working Group on
Biosafety (UNEP/CBD/ExCOP/1/2).
Expanding on its statement in the opening Plenary, the Like-Minded
Group reiterated the need to address related elements of Article 5
(Application of the AIA Procedure) of the ExCOP Draft Report in
discussions on scope. (Unless otherwise specified, references to
articles are as they appeared in the ExCOP Draft Report.) The EU
inquired about initiating discussions on the protocol’s relationship
with other agreements. Mayr announced that the contact group on scope
would address relevant elements of Article 5, but would not discuss
issues related to commodities. He further noted that Article 31
(Relationship with Other International Agreements) would be addressed
later.
The contact group on commodities commenced discussion on Article 17
(Information Sharing and the Biosafety Clearing-House) by drawing
attention to the proposed amendments in Chair Mayr’s non-paper. On
Article 15 (Handling, Transport, Packaging and Identification), the
group engaged in a conceptual discussion on the package proposal in
the text of the Draft Protocol contained in Annex II of the ExCOP
Draft Report. The group then discussed the package proposal paragraph
by paragraph. Delegates focused their discussion on Article 9 bis
(decision procedure for LMO-FFPs) in Chair Mayr’s non-paper,
particularly on language dealing with information provision subject to
domestic regulations. The group continued its discussion into the
night.
The contact group on scope met in the afternoon to discuss
outstanding issues related to Article 4 (Scope), where the negotiating
groups presented their general perspectives. Upon one group’s
proposal to start addressing the substance of the exemptions,
delegates discussed the status of pharmaceuticals for humans. During
an evening session, delegates continued discussions on the scope of
the protocol in relation to pharmaceuticals, contained use and
transit.
TUESDAY, 25 JANUARY 2000: On Tuesday delegates met during the
morning in the "Vienna setting" to hear contact groups’
reports on commodities and scope, as well as to begin a general
discussion on trade-related issues and the protocol’s relationship
with other international agreements. Chair François Pythoud
(Switzerland) of the contact group on commodities reported on Articles
15 and 17 of the ExCOP Draft Report stating that he would collaborate
with groups to present a Chair’s text. Regarding Article 9 bis (on
the decision procedure for the review of LMO-FFPs) in Mayr’s
non-paper, he noted progress on options for decision-making procedures
and capacity-building, bilateral agreements and cooperation between
Parties. Chair John Herity (Canada) of the contact group on scope
reported that negotiating groups provided complete explanations of
their positions on pharmaceuticals for humans, transit and contained
use. He also noted a proposal from the Like-Minded Group listing
articles that should not apply in these cases.
After a round of comments on the progress reports, Chair Mayr
stressed that discussions should focus only on the list of outstanding
items in the ExCOP Draft Report. Upon a request to raise outstanding
issues mentioned in official closing statements at the ExCOP in
Cartagena, Mayr suggested that the Legal Drafting Group could address
some of these issues. After a round of preliminary statements on the
cluster of trade-related issues, Chair Mayr closed the session so that
informal discussions on scope could proceed and the contact group on
commodities could meet.
The "Vienna setting" reconvened again in the evening to
hear reports of the contact groups. Chair Pythoud reported that the
contact group on commodities made progress and was close to a final
text in terms of concepts, but more time was required to find balanced
wording. Chair Herity reported that after informal discussions with
negotiating groups’ representatives on scope, the contact group
focused on transit. He noted general agreement on Article 4 (Scope)
and its coverage of all LMOs that may have adverse effects on
biodiversity. He said that new articles covering pharmaceuticals,
transit and notification were being developed. Chair Mayr convened a
new contact group under the chairmanship of Amb. Philémon Yang
(Cameroon) to address the cluster of trade-related issues and the
protocol’s relationship with other international agreements. He
stated that the contact group on commodities would continue to meet
and that discussions on scope would proceed informally under the
guidance of Chair Herity. The contact group on commodities reconvened
in the evening to continue discussing Articles 9 bis in Chair Mayr’s
non-paper and Article 15 of the ExCOP Draft Report. The contact group
on trade-related issues convened in the evening to address Articles 31
and 22 of the ExCOP Draft Report and their reformulation in Chair Mayr’s
non-paper.
WEDNESDAY, 26 JANUARY 2000: On Wednesday morning, delegates
reconvened in the "Vienna setting" to hear progress reports
from the contact groups. Chair Pythoud of the contact group on
commodities presented text on the decision procedure for LMO-FFPs,
claiming that groups were close to agreement. He noted that the group
also briefly discussed Annex 1B (Information Required in Notification)
contained in Chair Mayr’s non-paper. Chair Yang of the contact group
on trade-related issues reported on discussions on the use of
preambular language contained in Chair Mayr’s non-paper regarding
the Protocol’s relation to other international agreements. Chair
Herity of the contact group on scope reported that informal
consultations had not yet been resumed and proposed that they
continue. Mayr suggested that the contact groups on scope and
commodities be merged. He requested final text for presentation at a
late evening "Vienna setting." After discussion regarding
when to address the precautionary principle, Mayr stated that such
issues can be examined after the core issues are resolved.
The contact group on commodities met in a morning session to
discuss text proposed by the Chair on Article 18, particularly
regarding provisions on safety conditions, accompanying documentation
and declarations that movement of LMO-FFPs conform with the protocol’s
requirements. The contact groups on commodities and scope were then
merged and met in afternoon and evening sessions, where delegates
discussed a Chair’s summary text on scope, addressing
pharmaceuticals for humans, transit contained use. Co-Chairs Pythoud
and Herity later presented a revised text based on informal
consultations.
The contact group on trade-related issues and the Protocol’s
relationship with other international agreements met throughout the
day, where negotiating groups presented their initial views on the
issues. After a break in the evening session, Chair Yang distributed a
draft Chair’s text, deleting Articles 31 and 22 of the ExCOP Draft
Report and adding three preambular provisions with language from the
Rotterdam Convention on the Prior Informed Consent Procedure.
At 8:00 pm, Chair Mayr hosted a dinner for ministers arriving for
the final days of negotiations. At the dinner, Ministers heard remarks
from Chair Mayr as well as the Environment Minister of Canada, David
Anderson. The dinner set the stage for more informal discussions among
Ministers during the final two days of negotiations.
The "Vienna setting" convened at 11:20 pm to hear reports
of the contact groups and a round of views on the precautionary
principle. Mayr then requested that the contact groups on
trade-related issues, and commodities and scope meet to deliver text
to the "Vienna setting" on Thursday morning. Delegates
continued informal discussions on scope and commodities through
Wednesday night and into Thursday morning.
THURSDAY, 27 JANUARY 2000: On Thursday the contact group on
trade-related issues met at 9:00 am to continue discussions. The
"Vienna setting" convened at 1:00 pm, where Chair Mayr
requested all in attendance to stand, clasp hands, and ponder how to
move the process forward. The contact group Chairs then reported on
their progress. Chair Yang of the contact group on trade-related
issues reported that consultations continued on the basis of
preambular language proposed in the Chair’s draft text. Co-Chair
Herity of the contact group on scope and commodities reported that
some legal drafting issues had arisen in Article 4 (Scope) and that
acknowledgment of a state’s right to allow or prohibit the transit
of LMOs still required resolution. Co-Chair Pythoud reported that
discussions on Article 18 (Handling, Transport, Packaging and
Transportation) had almost achieved conceptual agreement, although
specific elements for identification still needed discussion. On the
decision procedure for LMO-FFPs, Pythoud reported that unresolved
issues included the decision procedure for countries without domestic
regulatory frameworks, implicit consent, and reference to the
precautionary approach.
At Chair Mayr’s request, negotiating groups commented on existing
proposals addressing the precautionary principle and other
trade-related provisions. Chair Mayr then expanded the mandate of the
contact group on relations with other international agreements and
non-discrimination to consider Article 8.7 on the precautionary
principle. He suggested that Pythoud serve as Co-Chair with Amb. Yang.
He requested text to review for the evening’s "Vienna
setting." Negotiating groups then listed items outside of the
core clusters that needed further consideration. Chair Mayr suggested
that negotiations continue to focus on the core issues, while informal
consultations conducted by Amb. Beat Nobs (Switzerland) take place on
other outstanding issues, including Articles 21, 23 and 24.
The contact group on trade-related issues met again in the
afternoon to continue discussions on the precautionary principle,
based on text contained in the ExCOP Draft Report. After initial
discussion, Chair Yang presented draft text on the precautionary
principle for further discussion.
At 10:00 pm the "Vienna setting" reconvened to hear
reports on trade-related issues and other outstanding items. Chair
Yang reported that the contact group deliberating the precautionary
principle was considering a draft text. Amb. Nobs reported on his
informal consultations, noting general agreement on Articles 15 (Risk
Assessment), 16 (Risk Management) and 25 (Illegal Transboundary
Movement), while outstanding issues remained on Articles 24
(Non-parties), 14 (Multilateral, Bilateral and Regional Agreements)
and 26 (Socio-economic Considerations). Chair Mayr requested Co-Chairs
Yang and Pythoud and Amb. Nobs to provide clean text by 2:00 am. He
then conducted informal consultations on the protocol’s text for
presentation at Friday morning’s "Vienna setting." The
contact group on trade-related issues continued discussions on
preambular language.
FRIDAY, 28 JANUARY 2000: On Friday, Chair Mayr opened the
"Vienna setting" at 10:30 am, noting that a draft text of
the Protocol with brackets on remaining issues had been distributed at
2:00 am, and that bilateral consultations had concluded at 5:45 am. He
expressed optimism that a final conclusion would be reached and was
considering how to bridge the remaining gaps. He stated his preference
to develop consensus text by the afternoon, however if this was not
possible, he would present the Plenary with a Chair’s text at 4:00
pm.
At 4:00 pm, it was announced that the final plenary would be
reconvened at 6:00 pm, which was then postponed to 9:00 and finally to
11:00 pm. Over this period, Chair Mayr facilitated informal
discussions with negotiating groups, primarily with regard to the
precautionary principle and preambular language on relations with
other international agreements.
CLOSING PLENARY
At 11:40 pm, President Mayr opened the closing plenary session. He
called Ilona Jepsen (Latvia), President of the Credentials Committee,
to submit the report on the credentials of representatives to the
resumed session of the ExCOP. Jepsen stated that 109 delegations were
in full compliance, seven delegations only partly complied, therefore
were not in good order, and 17 delegations had not submitted their
credentials. The report was provisionally adopted with the
understanding that delegations not in order should provide their
credentials within 30 days. At President Mayr’s request, rapporteur
Mariangela Rebuá (Brazil) submitted the report of the ExCOP in two
parts, from Cartagena and Montreal, included in documents UNEP/CBD/ExCOP/
1/L.2, UNEP/CBD/ExCOP/1/L.2/Add.1 and UNEP/CBD/ExCOP/1/ L.2/Add.2. The
reports were adopted by the ExCOP.
Chair Mayr then suspended the Plenary just before midnight to allow
for translation of the draft text and to resume consultations with
negotiating groups focusing on Article 18 and its provision for
identification and documentation for LMO-FFPs. Mayr reconvened the
Plenary at 4:40 am. He said delegates had resolved crucial problems
due to hard work and flexibility. He recommended adoption of the Draft
Cartagena Protocol on Biosafety (UNEP/CBD/ExCOP/1/L.5) with one
amendment to Article 18(a). The Protocol was adopted at 4:50 am. He
went on to say adoption of the protocol marked a victory for the
environment and for citizens of the entire world. UNEP Executive
Director Klaus Töpfer highlighted the historical significance of the
moment. He noted his deep admiration for Mayr and his dedicated staff.
He thanked all the "mothers and fathers" of the Protocol,
especially the ministers, BSWG Chair Veit Koester and the
international cadre of experts.
The Plenary then considered the draft decision (UNEP/CBD/ ExCOP/1/L.6)
on the adoption of the Cartagena Protocol on Biosafety and interim
arrangements submitted by the COP-4 Bureau. The decision consists of
four parts: adoption of the Protocol; establishment of the
Intergovernmental Committee for the Cartagena Protocol on Biosafety (ICCP);
establishment of a Roster of Experts for risk assessment and
management; and administrative and budgetary matters. FRANCE offered
to host the first meeting of the ICCP, before the end of the year
2000, which was adopted by the Plenary.
President Mayr then invited delegations to make closing statements.
Statements were made by Canada, Argentina, Uganda, Ethiopia, the EU,
Switzerland, Hungary, Burkina Faso, Japan, the US and Portugal. In
their statements, delegates thanked President Juan Mayr and his staff
for their hard work, as well as Montreal, Canada, and its citizens for
hosting the meeting. Many delegations expressed their appreciation to
the negotiating groups. Statements also referred, inter alia; to: the
Protocol’s role in the effective development of biotechnology;
support for capacity-building; the Protocol’s breakthrough on trade
and environment; and maintaining a balance among public concerns,
predictability for industry, and environmental protections. On behalf
of the majority of NGOs, the Third World Network noted that the
Protocol is the first instrument of international law to recognize the
distinct nature of LMOs and congratulated delegates for breaking
through the North-South/East-West divides to put the environment
before trade concerns. She expressed eagerness to work again with
delegates, especially on the issue of liability. The Global Industry
Coalition stated that the protocol would protect biodiversity, while
setting the direction to share the economic and social benefits with
the world.
President Mayr extended his warm gratitude to all in attendance and
adjourned the meeting at 6:00 am. After the Plenary, a brief
organizational meeting of the ICCP convened under the chairmanship of
Amb. Philémon Yang (Cameroon).
The Preamble contains
references to, inter alia: CBD Articles 19, (Handling of
Biotechnology and Distribution of its Benefits), 8(g) (Managing risks
of LMOs) and 17 (Exchange of Information); CBD COP Decision II/5
(Consideration of the Need for and Modalities of a Protocol for the
Safe Transfer, Handling and Use of LMOs); the precautionary approach;
the expansion of biotechnology and growing public concern over
potential effects on biodiversity and human health; the potential of
biotechnology for human well-being; the importance of centres of
origin and genetic diversity; and the limited capabilities of many
countries to cope with risks associated with LMOs; as well as
references to the Protocol’s relationship with other international
agreements and non-discrimination.
The contact group on former Articles 31 (Relationship with Other
International Agreements) and 22 (Non-discrimination) contained in the
ExCOP Draft Report, chaired by Amb. Philémon Yang (Cameroon),
addressed the cluster of trade-related issues and the relationship of
the Protocol with other international agreements. On Wednesday, 26
January, Chair Yang invited the negotiating groups to present their
views on these articles and the proposals in Chair Mayr's non-paper.
The non-paper proposed deleting the articles and reflecting their
content in the Preamble and a new paragraph in former Article 8
(Decision Procedure).
Regarding non-discrimination, some delegates considered a reference
to non-discrimination redundant, outside the CBD's scope and not
applicable to LMOs. Others stressed the importance of the principle of
non-discrimination for preventing conflicts between the Protocol and
other international agreements. During discussion on this issue one
group suggested removing the clause exempting Parties’ obligations
to existing international agreements where there might be serious
threat to biodiversity and asked for consideration of relevant issues
in Articles 24 (Non-Parties), 26 (Socio-economic Considerations) and
the precautionary principle, as contained in Article 10 (Decision
Procedure). Most delegates argued that the former Article 31 was
unacceptable, since it would subordinate the Protocol to international
trade agreements. A Chair's text deleted Articles 31 and 22 and
introduced three new preambular clauses borrowing language from the
Rotterdam Convention on the Prior Informed Consent Procedure.
The results of the group's discussions were presented in the
plenary on Wednesday and Thursday. The CEE and Compromise Group
approved of the proposed deletion and support for preambular language.
The Miami Group suggested deleting former Article 22 and indicated
they would consider the Chair’s proposed text, while the EU
suggested deleting former Article 31 and retaining former Article 22
and stated that Chair Mayr’s non-paper presents the most balanced
formulation of preambular language. The Like-Minded Group noted its
support for deleting both articles, and preference for preambular
language contained in the non-paper.
On Thursday, Chair Mayr expanded the mandate of the contact group
on Articles 31 and 22 to consider former Article 8.7 on the
precautionary principle. After lengthy discussion on the precautionary
principle during Thursday and Friday, delegates arrived at two
bracketed options for each of the following: mutual supportiveness
with other international agreements; and compatibility with other
international agreements. The final clause, noting the intention not
to create a hierarchy with other international agreements, was also
bracketed.
The final text, the result of informal consultations, includes
three new preambular clauses: the mutual supportiveness of trade and
environment agreements with a view to achieving sustainable
development; the statement that the Protocol shall not be interpreted
as implying a change in the rights and obligations of a Party under
existing international agreements; and the explanatory statement that
the above clause is not intended to subordinate the Protocol to other
international agreements.
ARTICLE 1 (Objective): The objective of the Protocol is to
contribute to ensuring an adequate level of protection in the field of
safe transfer, handling and use of LMOs resulting from modern
biotechnology that may have adverse effects on the conservation and
sustainable use of biodiversity. It references the precautionary
approach and risks to human health, and focuses on transboundary
movements.
ARTICLE 2 (General Provisions): This article outlines the general
obligations of Parties to the Protocol with regard to AIA and the
development, handling, transport, use, transfer and release of LMOs.
It reaffirms the sovereignty of States over their territorial sea and
accepts the rights of the Parties to take action that is more
protective of the conservation and sustainable use of biodiversity,
provided that such action is in accordance with other obligations
under international law, and is consistent with the objectives and
provisions of the Protocol.
In discussions on Article 18 (Handling, Transport, Packaging and
Identification), one group raised concern over the requirement for
Parties to ensure that the development, handling, transport, use,
transfer and release of any LMOs are undertaken in a manner that
prevents or reduces risk to biodiversity. After the informal
consultations on other issues conducted by Amb. Nobs this specific
requirement remained unchanged.
ARTICLE 3 (Use of Terms): This article contains definitions of, inter
alia: COP, contained use, export, exporter, import, importer, LMO,
regional economic integration organization, and transboundary
movement.
ARTICLE 4 (Scope): This article states that, in principle, the
Protocol applies to transboundary movement, transit, and handling and
use of all LMOs that may have adverse impacts on the conservation and
sustainable use of biodiversity, also taking into account risks to
human health. During the informal consultations, substantive
disagreements on scope were dealt with in a contact group chaired by
John Herity. At the end of the informal consultations, Herity noted
agreement to simplify Article 4 to include all LMOs. Discussions on
scope continued on the basis of a summary incorporating language from
the ExCOP Draft Report, Chair Mayr’s non-paper and a proposal by one
of the negotiating groups regarding exemptions. It was generally
decided to move provisions on pharmaceuticals, contained use and
transit to new articles.
ARTICLE 5 (Pharmaceuticals) [new article]: This article states that
the Protocol does not apply to the transboundary movement of LMOs that
are pharmaceuticals for humans and are addressed by other
international agreements or organizations. Parties are free to subject
all LMOs to risk assessment prior to decision-making on import.
During the informal consultations, the Miami Group noted that
pharmaceuticals generally may not have adverse impacts on
biodiversity, while the EU noted that international bodies governing
pharmaceutical issues could adequately address future developments. On
the first day of the resumed ExCOP, the contact group on scope
deliberated whether explicit reference to exemptions would compromise
the competence of the COP serving as the meeting of the Parties to
respond to future developments. (Note: Subsequent references to the
COP connote the COP serving as the meeting of the Parties, as
specified in Article 29.) Concern was expressed regarding developments
in pharmaceutical applications, such as gene-therapy, for which no
other standards or institutional provisions exist. The Like-Minded
Group supported including LMOs for pharmaceutical use and only
compromised to the extent that the decision could be left to the COP.
To address exemptions, a summary was produced containing a positive
and negative list of which articles should and should not apply to
LMOs intended as pharmaceuticals for humans as well as for LMOs in
transit. Ultimately, it was decided that LMOs intended as
pharmaceuticals for humans would be addressed by other relevant
international agreements or organizations.
ARTICLE 6 (Transit and Contained Use) [new article]: This article
states that LMOs for transit or contained use are excluded from the
AIA procedure without prejudicing the right of a Party of transit to
regulate the transport of LMOs through its territory or to subject
LMOs intended for contained use to risk assessments or national
standards.
During the informal consultations two main issues were considered:
the inclusion of advance notification and necessary documentation for
transit, and the need to specify and adjust the definition of
contained use. On Monday, informal consultations between
representatives of the negotiating groups focused on transit and the
practical and logistical burdens of adhering to notification for
countries of transit. After continued discussions on Tuesday and
Wednesday, it was decided that the AIA procedure should not apply to
LMOs in transit and LMOs for contained use.
ARTICLE 7 (Application of the Advance Informed Agreement Procedure)
[formerly Article 5]: This article states that, subject to Articles 5
(Pharmaceuticals) and 6 (Transit and Contained Use), the AIA
procedure, contained in Articles 8, 9, 10 and 12, shall apply prior to
the first transboundary movements of LMOs for intentional introduction
into the environment of the Party of import. It further states that
intentional introduction into the environment does not refer to
LMO-FFPs, which are governed by Article 11 (Procedure for LMO-FFPs).
It also states that the AIA procedure shall not apply to the
intentional transboundary movement of LMOs identified in a COP
decision as being unlikely to have adverse effects on the conservation
and sustainable use of biodiversity, taking also into account risks to
human health.
ARTICLE 8 (Notification) [formerly Article 6]: This article states
that the Party of export shall notify or require the exporter to
ensure notification in writing to the importer's competent national
authority prior to the intentional transboundary movement of an LMO
covered by the AIA procedure in Article 7. The notification shall
contain, at a minimum, the information specified in Annex I
(Information Required in Notification).
ARTICLE 9 (Acknowledgement of Receipt of Notification) [formerly
Article 7]: This article states that the Party of import shall
acknowledge receipt of a notification, in writing, within 90 days of
its receipt. The content of the acknowledgement must include: date of
receipt; whether the notification, prima facie, contains the
information referred to in Article 8 (Notification); and whether to
proceed according to the domestic regulatory framework of the Party of
import, provided that it is consistent with the Protocol or according
to Article 10 (Decision Procedure). The article specifies that failure
to acknowledge receipt shall not imply consent for transboundary
movement.
ARTICLE 10 (Decision Procedure) [formerly Article 8]: This article
requires Parties of import to inform the notifier, within a 90-day
period that the transboundary movement may proceed, either only after
written consent, or without subsequent written consent. Parties are
required to communicate their decision within 270 days of receipt of
notification to the notifier and the Biosafety Clearing-House. The
article then sets out four possible decisions that Parties may take:
approval, including how the decision applies to subsequent
imports;
prohibition;
request for additional information; or
information that the 270-day timeframe has been extended by a
defined period of time.
The article specifies that a failure by a Party to communicate its
decision within 270 days shall not imply consent. Parties must give
reasons for their decision, except for unconditional approval.
Appropriate procedures and mechanisms to facilitate decision-making
will be determined by the first COP to the Protocol.
The issue of the precautionary principle contained in former
Article 8.7, was raised during the "Vienna setting" on
Wednesday and Thursday, when Mayr asked negotiating groups to comment
on existing proposals addressing it in relation to Articles 31, 22 and
alternative preambular language. The Miami Group indicated that
references in the Preamble, Article 1 (Objective) and Annex II (Risk
Assessment) were sufficient and that operationalization in former
Article 8 was not necessary. The EU, Compromise Group, CEE and
Like-Minded Group supported the existing provision in former Article
8.7. The EU stressed that, while decisions should be based on
science-based risk assessment and non-arbitrariness, governments
should have the sovereign right to take decisions to avert
irreversible damage. The Like-Minded Group stated that referring to
the precautionary principle solely in the Preamble would be
unacceptable.
Discussions on the precautionary principle continued in a contact
group on the basis of the text contained in the ExCOP Draft Report.
One group stated that the AIA procedure forms the core of the Protocol
and that the precautionary principle, as part of the decision
procedure, should be adequately reflected in its operational
provisions. Another group stated that reference to "adverse
effect" was unclear, as well as the basis on which an importing
country could prohibit an import. A proposal by one of the negotiating
groups suggesting new language for the article was submitted and used
as the basis for discussion. The text included two sections, one on
the precautionary approach regarding import of LMOs, and another on
review of actions taken by the Party of import in case of availability
of additional scientific information. Negotiating groups agreed to
delete language on the review of action by the Party of import.
During a line-by-line analysis of the provision, discussion
addressed two issues: the basis on which a Party of import would be
allowed to prohibit import of LMOs; and the criteria for a solid
scientific basis to trigger an importing Party to take actions against
the import of LMOs. No consensus was reached and the Chair presented a
draft text for the provision based on the discussions.
The draft text suggested two options: the first stated that Parties
of import may have to take decisions on the import of LMOs in order to
minimize possible adverse effects, even in the absence of scientific
certainty. The second option generally stated that lack of scientific
certainty shall not prevent the Party of import from taking a
decision. The meeting was adjourned and the two options remained
bracketed.
Following Friday's informal negotiations, the first option
prevailed: Article 10.6 (former Article 8.7) permits importing Parties
to invoke the precautionary approach, which states that lack of
scientific certainty due to insufficient information of the potential
adverse effects on biodiversity shall not prevent a Party from taking
a decision on the import of an LMO. The provision also allows Parties
to take into risks to human health. The same issue was addressed with
regard to LMO-FFPs in Article 11.8. A provision on the circumstances
to be defined by concerned Parties, under which transboundary
movements can take place without written consent, was deleted as a
result of Friday's informal negotiations.
ARTICLE 11 (Procedure for LMO-FFPs) [formerly Article 9 bis
in Chair Mayr’s non-paper]: Article 11 outlines the notification and
decision process for LMOs intended for direct use for food or feed, or
for processing (LMO-FFPs), including provisions, inter alia,
on: notification of the Biosafety Clearing-House for LMO-FFPs placed
on the market; exemption of field trials for LMO-FFPs; decisions on
import of LMO-FFPs under domestic regulatory frameworks consistent
with the Protocol; countries lacking domestic regulatory frameworks
for LMO-FFPs; the precautionary principle; and developing countries’
need for capacity-building with respect to LMO-FFPs.
During the informal consultations, negotiating groups started
discussions based on Article 9 bis proposed in Mayr’s
non-paper. The Like-Minded Group expressed concern over the
possibility of enabling implicit consent in Article 9 bis. The
Miami Group noted general satisfaction with the non-paper's proposal,
recognized the importance of information-sharing and documentation
regarding transboundary movement of LMO-FFPs, but emphasized that the
AIA procedure must be workable and that decision-making procedures
should consider domestic legislation more fully. The CEE stressed the
need to apply the AIA to all LMOs, and preferred a separate paragraph
dealing with LMO-FFPs. The EU stated that the non-paper's proposal for
an alternative system was useful, and, supported by other groups,
suggested moving the alternative AIA procedure to follow former
Article 8. The Compromise Group noted that failure to respond should
not imply consent. He also highlighted that application of AIA be
based on risk assessment and capacity-building. A contact group on
commodities was established to consider this and other issues.
On Sunday, contact group Chair François Pythoud reported that new
text for Article 9 bis covered information requirements
regarding transboundary movements of LMO-FFPs, the timeframe and the
means of providing such information in advance. Two separate
paragraphs were developed to address additional information
requirements, financial and technical assistance and capacity-building
in this area. In summarizing the decision procedures for LMO-FFPs,
Pythoud noted the group's understanding that the main basis for
decisions would be domestic regulation, although groups differed on
the procedure to be followed in the absence of domestic regulations.
The Like-Minded Group affirmed that language on domestic regulations
and decisions on imports of LMO-FFPs still remained to be discussed.
On Tuesday, Chair Pythoud requested that negotiating groups
continue discussions on the text he presented on Article 8 bis,
which had formerly been referred to as 9 bis. One group
suggested deleting a reference to consistency with this protocol
because there was no need for standardized domestic regulatory
frameworks. Other groups disagreed. In the effort to solve this
problem, the following suggestions were made: referring to consistency
with the objective of the Protocol; referring specifically to Articles
12 (Risk Assessment) and 13 (Risk Management); or using domestic
frameworks "compatible" with the protocol.
New text merging the Chair's provisions, referring to Parties with
regulatory frameworks and Parties lacking regulatory frameworks, was
presented to the contact group. One group described the rationale
behind the merger as capturing all the concepts in the original
paragraphs, while not creating a duality between Parties that do and
Parties that do not have regulatory frameworks. Some participants
expressed disappointment with the merged text, saying that it:
complicated the decision-making process, created redundancy with other
paragraphs, introduced too many new ideas, and moved the discussion
backwards. On language in the Chair's text stating that an importing
Party's failure to communicate its decision does not imply consent,
some expressed concern that it was too prescriptive since it did not
recognize that some countries' domestic regulations could allow for
implicit consent. The contact group drafted new text to accommodate
this concern.
On Thursday, Pythoud reported to the "Vienna setting,"
that a number of issues remained unresolved, including: the decision
procedure for countries without domestic regulatory frameworks;
implicit consent; and reference to the precautionary approach. He said
he would continue bilateral and multilateral consultations with
negotiating groups to resolve the remaining problems. The outstanding
issues were addressed during the final informal consultations on
Thursday and Friday and were finally reflected in Article 11 of the
final Protocol text.
ARTICLE 12 (Review of Decision) [formerly Article 9]: This article
permits a Party of import to review and change its decision regarding
the transboundary movement of an LMO at any time. The Party of import
must base its decision on new scientific information, taking into
account risks to human health. The Party must then inform the notifier
and the Biosafety Clearing-House within 30 days, giving reasons for
the decision. The article also sets out under what conditions a Party
of export or notifier may request a review, where it considers that a
change of circumstances has occurred or that additional scientific or
technical information is available. Parties of import are required to
respond to requests for review within 90 days. Finally, the article
provides for a Party of import to require risk assessments for
subsequent LMO imports, at its own discretion.
ARTICLE 13 (Simplified Procedure) [formerly Article 10]: This
article allows a Party of import to specify in advance, to the
Biosafety Clearing-House, LMOs to be exempted from AIA, as well as
when transboundary movements may proceed simultaneously with
notification, in which case such notifications would apply to
subsequent movements to the same Party.
ARTICLE 14 (Bilateral, Regional and Multilateral Agreements and
Arrangements) [formerly Article 11]: This article sets out provisions
applying to Parties who enter into multilateral, bilateral and
regional agreements and arrangements with Parties or non-Parties
regarding procedures for transboundary movements of LMOs, which must
be consistent with the objectives of the Protocol, and not result in a
lower level of protection than provided by the Protocol. The article
also requires notification of the Biosafety Clearing-House of such
agreements and allows for an importing Party to determine that its
domestic regulations shall apply to imports, provided that it notify
the Biosafety Clearing-House.
ARTICLE 15 (Risk Assessment) [formerly Article 12]: This article
sets out the provisions under which risk assessment will be carried
out. It says that risk assessment shall be undertaken in accordance
with the provisions in Annex II and be based, at a minimum, on
information provided in accordance with the notification procedure and
other available scientific evidence in order to identify and evaluate
the possible adverse effects of LMOs on the conservation and
sustainable use of biodiversity, taking also into account the risks to
human health. The text also states that the importer shall ensure that
risk assessment is carried out in accordance with the AIA procedure,
but that the importer may require the exporter to carry out risk
assessment. Finally, it requires the notifier to bear the financial
responsibility for risk assessment.
This article in the ExCOP Draft Report was revisited by Amb. Nobs’
informal consultation, and minor linguistic amendments were made.
ARTICLE 16 (Risk Management) [formerly Article 13]: This article
states that Parties shall establish and maintain appropriate
mechanisms, measures and strategies to regulate, manage and control
risks identified under the risk assessment provisions, and elaborates
on the measures and controls. The measures shall be imposed to prevent
adverse effects on biodiversity, and Parties can require risk
assessments prior to the first release of an LMO. The article also
states that each Party shall, in order to ensure genomic and trait
stability, endeavor to ensure that any LMO undergoes a period of
observation commensurate with its life-cycle or before being put to
its intended use. Finally, the article states that Parties shall
cooperate in identifying LMOs or specific LMO traits that may have
adverse effects on biodiversity, taking into account risks to human
health, with a view to taking appropriate measures on the treatment of
such LMOs.
ARTICLE 17 (Unintentional Transboundary Movements and Emergency
Measures (formerly Article 14): This article details the measures that
Parties are to take in the event of unintentional transboundary
movements of LMOs, including notification, provision of information
and consultation.
ARTICLE 18 (Handling, Transport, Packaging and Identification)
[formerly Article 15]: This article sets out procedures for the
packaging and identification of LMOs to be transported across national
boarders, and addresses, inter alia: measures to ensure that
LMOs are handled, packaged and transported under safe conditions and
relevant international standards, and three differentiated minimum
documentation requirements for LMO categories.
On Monday, contact group Chair Pythoud initiated conceptual
discussions on the "package proposal" contained in Annex II
of the ExCOP’s Draft Report. The significance of documentation
requirements to the implementation of the Protocol was highlighted.
Discussions focused on how proper documentation helps Parties reduce
damage in case of accidents and that without documentation, Parties
are unable to identify whether the Protocol's provisions have been
respected. One participant proposed that LMOs be divided into three
categories in this regard: LMOs to be released into the environment
requiring stringent documentation requirements; LMOs for contained use
that should be clearly identified; and LMO-FFPs that should be
indicated as such. Others emphasized that all LMOs should be
identified, and documentation should not only apply to the first
transboundary movement, but also to subsequent movements. One group
expressed its concern over the differentiated treatment of LMO-FFPs in
terms of documentation, and highlighted that documentation
requirements must be workable for commercial actors. One group said
that this article is closely linked with other issues such as
commodities and the scope of the Protocol, and that since his group
viewed the ExCOP Draft Report as more balanced, discussion on this
article should not be reopened.
Conceptual difficulties were expressed regarding time frames and
whether LMOs currently traded in the marketplace would be subject to
the same identification requirements. Participants expressed views on
the degree of certainty a Party can expect regarding the percentage of
LMO content in a given shipment. Some suggested that a threshold
regarding what percentage of LMO content requires identification does
not exist and raises difficult legal questions. Others indicated that
it is impossible to know the final destination of a shipment of LMOs
or the exact quantity of LMOs in a given shipment, hence
identification requirements are not obvious. In closing the discussion
on the package proposal, some expressed their desire to retain ExCOP
draft text while others wished to further explore a revised text based
on the package proposal.
Based on discussions in the contact group, Pythoud presented a
Chair’s draft text on Wednesday reflecting all the principles in the
EXCOP Draft Report, while allowing for flexibility when dealing with
different categories of LMOs. Delegates addressed a provision on the
safety conditions of LMOs when handled, packaged and transported.
Certain groups expressed concern that the application of safety
measures required qualification on a case-by-case basis and that they
should only be applied "as appropriate."
On accompanying documentation requirements during the transport of
LMOs, some groups stressed that documentation was a minimum
requirement. There was discussion on ensuring that the provision
covered not only the first, but also subsequent movements of LMOs.
Negotiating groups confirmed the need for documentation identifying
LMO-FFPs, but disagreed on exactly how LMO-FFPs should be identified.
One group proposed that "any unique identification" in
addition to "identity" of LMO-FFPs be specified. Another
supported identification of LMO-FFPs "as not intended for
intentional introduction into the environment." One group noted
difficulties with the documentation requirements for LMO-FFPs, and
requested the proposals be bracketed. Another questioned the
appropriateness and clarity of a provision requiring a declaration
that the movement of LMO-FFPs conform with the Protocol's
requirements. To clarify who should make the declaration, one group
suggested the provision should apply only to exporters. The provision
was bracketed.
One group stated that a provision requiring the meeting of the
Parties to consider the need for and modalities of developing
standards with regard to identification, handling, packaging and
transport was unnecessary. One group stated that a reference to
collaboration with other international bodies undermines the CBD and
the Protocol and suggested language referring to consultations with
other international bodies used in the ExCOP Draft Report. As
suggested by the Chair, the group agreed to bracket the entire
provision with this amendment. As the contact group’s discussion
drew to a close, conceptual agreement had almost been achieved and the
negotiating groups had agreed to a differentiated approach to
accompanying documentation for LMOs and, in principle, to identifying
LMO-FFPs. However, the specific identification requirements remained
outstanding. Consultations with negotiating groups to resolve the
remaining issues continued.
During the closing Plenary, Mayr presented the final draft Protocol
and requested its adoption after changes to the this article regarding
documentation requirements. The changes stipulated that documentation
for shipment of LMO-FFPs should state that they "may
contain" LMOs and are not intended for introduction into the
environment. The COP is directed to take a decision on the detailed
requirements, including identity and any unique identifications,
within two years.
ARTICLE 19 (Competent National Authority and National Focal Point)
[formerly Article 16]: This article requires governments to designate
national focal points and competent national authorities to liaise
with the Secretariat and perform administrative functions under the
Protocol.
ARTICLE 20 (Information Sharing and the Biosafety Clearing-House)
[formerly Article 17]: This article establishes a Biosafety
Clearing-House and outlines its objectives and the types of
information that should be provided to it. Modalities of the operation
of the Clearing-House shall be considered and decided upon by the COP
serving as the meeting of the Parties at its first meeting, and kept
under review thereafter.
The contact group on commodities focused on whether Parties shall
be required to provide information regarding the transboundary
movement of LMO-FFPs and exemptions from AIA procedures according to
Articles 4, 5 and 6 to the Clearing-House. Chair Pythoud commenced
discussion on this article by drawing attention to the proposed
amendments in Chair Mayr’s non-paper. One group claimed that a
broader range of information requirements regarding national
legislation is reflected in the ExCOP Draft Report than in the
non-paper proposal. He noted that it is not necessary to limit
information on national legislation to implementation of the protocol.
Another group noted that the amendment regarding information
requirements for LMO-FFPs in domestic regulations repeats a proposed
new article on decision procedure of LMO-FFPs in Chair’s Mayr’s
non-paper. Negotiating groups agreed to ignore the proposed amendments
in the non-paper and retain the text contained in the ExCOP Draft
Report.
ARTICLE 21 (Confidential Information) [formerly Article 18]: This
article provides for the Party of import to permit the notifier to
identify information that should be treated as confidential. It
identifies information that "may not" be considered
confidential, such as the general description of the LMOs, the name
and address of the notifier, a summary of the risk assessment
undertaken and plans for emergency response.
ARTICLE 22 (Capacity-building) [formerly Article 19]: This article
states that Parties shall cooperate in the development and
strengthening of human resources and institutional capacities in, inter
alia: safe biotechnology management training, risk assessment and
management; technological and institutional capacities; and
biotechnology to the extent that it is required for biosafety. The
article references the needs of developing country Parties, in
particular the least developed and small island developing States, as
well as countries with economies in transition.
ARTICLE 23 (Public Awareness and Participation) [formerly Article
20]: This article requires Parties to promote and facilitate public
awareness, education and participation in the Protocol’s
implementation. It requires consultation with the public in the
decision-making process and provision of results to the public, while
respecting confidential information. It calls on each Party to inform
its public about how to access the Biosafety Clearing-House.
ARTICLE 24 (Non-Parties) [formerly Article 21]: This article states
that transboundary movements of LMOs between Parties and non-Parties
shall be consistent with the Protocol’s objective, and Parties may
enter into bilateral, regional and multilateral agreements and
arrangements with non-Parties regarding such transboundary movements.
It also requires Parties to encourage non-Parties to adhere to the
Protocol and contribute appropriate information to the Biosafety
Clearing-House. During the informal consultations conducted by Amb.
Nobs on other outstanding issues, delegates debated the wording with
regard to transboundary movements between Parties and non-Parties.
Amb. Nobs’ informal consultations made minor linguistic changes.
ARTICLE 25 (Illegal Transboundary Movements) [formerly Article 23]:
This article obliges Parties to adopt appropriate domestic measures to
prevent and penalize transboundary movements of LMOs carried out in
contravention of domestic measures to implement this Protocol. It
empowers the Party affected by illegal transboundary movement to
request the Party of origin to dispose of the LMOs at its own cost. It
also requires Parties to make available to the Biosafety
Clearing-House information concerning cases of illegal transboundary
movement. During informal consultations conducted by Amb. Nobs,
general edits in legal drafting were made.
ARTICLE 26 (Socio-economic Considerations) [formerly Article 24]:
This article allows Parties to take socio-economic considerations
arising from the impact of LMOs on the conservation and use of
biodiversity into account in reaching decisions on whether to allow
imports of LMOs. Such decisions are to be consistent with the Parties’
international obligations. It encourages Parties to cooperate in
research and information exchange on socio-economic impacts. The
amendment made by the informal consultations conducted by Amb. Nobs
included a reference to Parties’ domestic measures to implement the
Protocol with regard to socio-economic considerations.
ARTICLE 27 (Liability and Redress) [formerly Article 25]: This
article states that the first COP serving as the meeting of the
Parties shall adopt a process with respect to the appropriate
elaboration of international rules and procedures in the field of
liability and redress for damage resulting from transboundary
movements of LMOs. The COP will take into account any ongoing
processes in international law on these matters and shall endeavor to
complete this process within four years.
ARTICLE 28 (Financial Mechanism and Resources) [formerly Article
26]: This article establishes the financial mechanism of the CBD as
that of the Protocol and, with regards to guidance to the mechanism,
references the need for capacity-building and financial resources for
developing countries. The COP serving as the meeting of the Parties to
the Protocol shall provide such guidance to the COP of the CBD to
consider and forward to the financial mechanism.
ARTICLE 29 (Conference of the Parties serving as the Meeting of the
Parties) [formerly Article 27]: This article states that the COP to
the CBD shall serve as the meeting of the Parties to the Protocol and
shall keep under review implementation of the Protocol.
ARTICLE 30 (Subsidiary Bodies) [formerly Article 28]: This article
states that any subsidiary body under the CBD may serve the Protocol
upon a decision of the COP serving as the meeting of the Parties.
ARTICLE 31 (Secretariat) [formerly Article 29]: This article states
that the CBD Secretariat shall serve as the secretariat to the
Protocol.
ARTICLE 32 (Relationship with the Convention) [formerly Article
30]: This article states that the provisions of the CBD shall apply to
the Protocol, except as otherwise provided in the Protocol.
ARTICLE 33 (Monitoring and Reporting) [formerly Article 32]: This
article states that each Party shall monitor the implementation of the
Protocol and report to the COP on measures taken.
ARTICLE 34 (Compliance) [formerly Article 33]: This article states
that the first COP serving as the meeting of the Parties to the
Protocol shall consider and approve cooperative procedures and
institutional mechanisms to promote compliance and address
non-compliance.
ARTICLE 35 (Assessment and Review) [formerly Article 34]: This
article provides that the COP serving as the meeting of the Parties
shall evaluate the Protocol's effectiveness, including its procedures
and annexes, five years after its entry into force and every five
years thereafter.
ARTICLE 36 (Signature) [formerly Article 35]: This article states
that this Protocol shall be open for signature in Nairobi by States
and regional economic integration organizations from 15 to 26 May
2000, and at UN Headquarters in New York from 5 June 2000 to 4 June
2001.
ARTICLE 37 (Entry into Force) [formerly Article 36]: This article
states that this Protocol shall enter into force on the ninetieth day
after the date of deposit of the fiftieth instrument of ratification,
acceptance, approval or accession by States or regional economic
integration organizations that are Parties to the Convention.
ARTICLE 38 (Reservations) [formerly Article 37]: This article
states that no reservations may be made to the Protocol.
ARTICLE 39 (Withdrawal) [formerly Article 38]: This article states
that a Party may withdraw from the Protocol after two years from the
date on which this Protocol has entered into force for a Party.
ARTICLE 40 (Authentic Texts) [formerly Article 39]: This article
states that the original of this Protocol shall be deposited with the
UN Secretary-General.
ANNEX I (Information Required in Notifications under Articles 8, 10
and 13): This annex provides a list of biosafety-related information
required in notifications, including, inter alia:
contact information on the importer and exporter;
name and identity of the LMOs;
intended date of the transboundary movement;
taxonomic information requirements;
information on centers of origin and genetic diversity of the
recipient organism and/or the parental organisms;
description of the nucleic acid or the modification introduced,
the technique used, and the resulting characteristics of the LMOs;
intended use of the LMO or products thereof;
quantity or volume of the LMOs;
a previous and existing risk assessment report;
suggested methods for safe handling, storage, transport and use;
regulatory status of the LMO within the exporting State;
result and purpose of any notification by the exporter to other
States regarding the LMOs to be transferred; and
declaration that the above-mentioned information is factually
correct.
The contact group on commodities based their discussion on a new
proposed text (Annex IB) in Chair Mayr’s non-paper. Delegates agreed
that several new elements should be added to the list, including, inter
alia, description of the nucleic acid of LMOs, unique
identification of LMOs, and suggested methods for safe handling,
storage and transport and use, including labeling and documentation.
Many elements from Annex I of the ExCOP Draft Report were also
retained.
ANNEX II (Risk Assessment): This annex includes more specific
detail on risk assessment, including: objective, use, general
principles, methodology, and points to consider (e.g., recipient or
parental organism, donor organism, vector, insert and/or
characteristics of modification, LMO, detection and identification,
information on intended use, and receiving environment).
ANNEX III (Information Required for LMO-FFPs under Article 11):
This annex was added and includes a list for information required for
LMO-FFPs under Article 11. Such information includes, inter alia:
contact information on the applicant for a decision;
contact information of the authority responsible for the
decision;
name and identity of the LMO;
description of the gene modification, technique used and
resulting characteristics of the LMO;
any unique identification;
taxonomic information on the recipient and donor organisms;
information on centers of origin and genetic diversity of the
recipient organism and/or the parental organisms;
approved uses of the LMO;
a risk assessment report consistent with Annex II; and
suggested methods for safe handling, storage, transport and use.