INTRODUCTION
1. In considering the progress and effectiveness
of non-proliferation regimes to counter weapons of mass destruction,
it is not easy to focus from a western viewpoint on the security
regimes and not recognise that in the poorer developing countries,
concerns are much less security-driven and much more about health
and the environment and their economic prosperity. In addition,
the World Health Organization (WHO) and its corresponding animal
and plant health organizations, the Office International des Epizooties
(OIE) and the Food and Agriculture Organization (FAO) have disease
surveillance and reporting requirements which are also relevant
to enhancing transparency and building confidence.[17]Consequently,
to achieve universal non-proliferation regimes it is important
to recognize that there are other relevant regimes which are of
greater relevance to the developing countries. The challenge is
to devise non-proliferation regimes which bring benefits to all
Statesboth developed and developing.
2. This is especially true in respect of
the non-proliferation regimes for both biological and chemical
weapons. It will be recalled that both the Biological and Toxin
Weapons Convention (BTWC) and the Chemical Weapons Convention
(CWC) embody a "general purpose criterion" in their
basic prohibition. Thus Article I of the BTWC states that:
(1) Microbial or other biological agents, or
toxins, whatever their origin or method of production, of types
and in quantities that have no justification for prophylactic,
protective or other peaceful purposes;
(2) Weapons equipment or means of delivery designed
to use such agents or toxins for hostile purposes or in armed
conflict.
The general purpose criterion is in bold. In
the CWC, the general purpose criterion comes in the definition
of chemical weapons in Article II:
3. These general purpose criteria in the
BTWC and the CWC ensure that any microbial or other biological
agent of toxic chemical that is not intended for permitted purposes
is prohibited. The general purpose criteria thereby ensure that
the two conventions are all embracing and include both past and
future biological and chemical agents. It needs to be emphasised
that the chemical and biological agents that are generally recognised
as having been put into chemical and biological weapons are but
a selection of a much wider range of chemicals and of biological
materials that can cause harm to humans, animals or plants.
4. It is therefore, relevant and important
to also consider the other control regimes which States have introduced
to protect their populations from dangerous chemicals or from
microbial agents and genetically modified organisms. It is important
to recognise the growing pressures for a cleaner and healthier
environment that are driving towards greater controls of chemical
and biological materials that may present a hazard to human health
or the environment. These other control regimes have also been
evolving over the past few decades and need to be taken into account
when examining the development of non-proliferation regimes as
these other control regimes are frequently highly regarded by
the developing countries. These security and other control regimes
can conveniently be summarised graphically.
The evolution of these control regimes for "banned
and severely restricted" chemicals and for genetically modified
organisms are addressed below.
BANNED AND
SEVERELY RESTRICTED
CHEMICALS
5. The world growth in trade in chemicals
during the 1960s and 1970s has led to increasing concerns about
the risks of using hazardous chemicals and thus to the recognition
of the need to exchange and make available information about such
chemicals. A multilateral exportimport system for banned
and severely restricted toxic chemicals has been developed which
has National Authorities in 155 countries administering a voluntary
exportimport system.[18]
Since 1992, this regime had been the subject of a legally binding
European Community Regulation.[19]
Recently, the Rotterdam Convention on the Prior Informed Consent
(PIC) Procedure for Certain Hazardous Chemicals and Pesticides
in International Trade was negotiated and adopted as a legally
binding instrument on 10 September 1998. This will enter into
force once 50 States have ratified it.
United Nations Consolidated List
6. Following the growth in world trade in
chemicals in the 1960s and 1970s, the Governing Council of the
UN Environment Programme (UNEP) in 1977 urged[20]
Governments to take steps to ensure that potentially harmful chemicals,
which are unacceptable for domestic purposes in the exporting
country, are not permitted to be exported without the knowledge
and consent of appropriate authorities in the importing country.
7. Some five years later, the United Nations
General Assembly "aware of the damage to health and the environment
that the continued production and export of products that have
been banned and/or permanently withdrawn on ground of human health
and safety ....is causing in the importing countries and"
"considering that many developing countries lack the necessary
information and expertise to keep up with developments in this
field" requested[21]
that the Secretary-General prepare and regularly update "a
consolidated list of products whose consumption and/or sale have
been banned, withdrawn, severely restricted or not approved by
Governments." This list is prepared[22]
and regularly updated jointly by the United Nations, the World
Health Organisation and the United Nations Environmental Programme/International
Register of Potentially Toxic Chemicals (UNEP/IRPTC). This is
part of a continuing effort in the United Nations system aimed
at disseminating information internationally on products harmful
to health and the environment. It provides information on restrictive
regulatory decisions taken by Governments on pharmaceutical, agricultural
and industrial chemicals, and consumer products. The Fourth Edition
covers regulatory actions taken by 92 Governments on over 600
products. The introduction to the Fourth Edition notes that "It
is important to realize that all pharmaceutical and chemical products
are potentially harmful if not correctly used "and that"
The list does not include many widely used industrial chemicals
to which occupational exposure limits have been assigned by national
authorities, and on which information is available on ILO (International
Labour Organisation) and UNEP/IRPTC publications."
8. In order to ensure that the list focuses
on products harmful to health and the environment, criteria for
the inclusion of products were developed in 1985 and transmitted
to Governments for their comments. These criteria, revised in
the light of the comments received, are reproduced in an Annex
to the Consolidated List. Those for chemical products are "Banned",
"Withdrawn" and "Severely restricted" which
are defined as:
The London Guidelines
9. UNEP in 1987 adopted[23]
the London Guidelines for the Exchange of Information on Chemicals
in International Trade[24]
which were aimed at enhancing the sound management of chemicals
through the exchange of scientific, technical, economic and legal
information. Special provisions were included regarding "the
exchange of information on banned and severely restricted chemicals
in international trade, which call for cooperation between exporting
and importing countries, in the light of their joint responsibility
for the protection of human health and the environment at the
global level." UNEP in adopting these guidelines also identified
that additional measures were required to enable importing countries
to give or withhold their consent to particular exports following
receipt of adequate information from exporting countries and that
such measures, based on the principle of prior informed consent
should be incorporated in the London Guidelines as expeditiously
as possible.
10. This principle of Prior Informed Consent
(PIC) was incorporated[25]
in the amended London Guidelines[26]
in 1989. These provide a mechanism for importing countries to
formally record and disseminate their decisions regarding the
future importation of chemicals which have been banned or severely
restricted in the exporting countries and outlines the shared
responsibilities of importing and exporting countries and exporting
industries in ensuring that these decisions are heeded. The Introduction
to the Guidelines states that "Although these Guidelines
have not been prepared specifically to address the situation of
developing countries, they nevertheless provide a framework for
the establishment of procedures for the effective use of chemicals
in these countries. Implementation of the Guidelines should thus
help them to avoid serious and costly health and environmental
problems due to ignorance about the risks associated with the
use of chemicals, particularly those that have been banned or
severely restricted in other States."
11. The PIC procedure is being implemented jointly
by the Food and Agriculture Organization (FAO) of the United Nations
which leads for pesticides and UNEP through the IRPTC (International
Register of Potentially Toxic Chemicals) which leads for chemicals.
Each participating countryof which, by 30 June 1998, there
are 155nominates a Designated National Authority (DNA)
to serve as a focal point for the operation of the PIC procedure.
Some countries have designated one authority for all chemicals
while others have designated two, one with the responsibility
for pesticides and the other for other chemicals. The DNA is generally
a government department or office responsible for broad policy
decisions with the authority to decide which chemicals may be
used in the country. In the UK, it is the Chemicals and Biotechnology
Division of the Department of the Environment while in the USA
it is the Assistant Administrator, Prevention, Pesticides and
Toxic Substances of the Environment Protection Agency.[27]
12. The functions of the DNA in respect
of the import of banned or severely restricted chemicals are to
receive information on exports from exporting States, to transmit
requests for further information as required to exporting States,
to advise and assist import control authorities, to strengthen
national decision-making procedures and import control mechanisms,
to ensure that decisions apply uniformly to all import sources
and to domestic production of chemicals for domestic use, and
to encourage that chemicals subject to PIC be purchased only from
sources in exporting countries which are participants in that
procedure. Insofar as exports of banned or severely restricted
chemicals are concerned, the function of the DNA is to ensure
the provision or transmittal of information on exports, to respond
to requests for information from other States, especially as regards
sources of precautionary information on the safe use and handling
of the chemicals concerned, to communicate PIC decisions to their
export industry, and to implement appropriate procedures, within
their authority, designed to ensure that exports do not occur
contrary to the PIC decisions of participating importing countries.
13. Participating countries provide information
on control actions they have taken to ban or severely restrict
chemicals by completing a Notification of Control Action form
which gives competent authorities in other States the opportunity
to assess the risks associated with the chemical and to make timely
and informed decisions thereon having regard to local environmental,
public health, economic and administrative conditions. The minimum
information to be provided is the chemical identification/specification
of the chemical, a summary of the control action taken and the
reasons for it and whether additional information is available.
The reasons supporting the control action should be based on a
national review of scientific data, information or analysis which
indicate that use under expected conditions within the country
may give rise to an unacceptable risk to human health or the environment.
Any chemical banned or severely restricted in at least one country
after 1 January 1992 is eligible for inclusion in the PIC procedure;
any chemicals banned or severely restricted prior to that date
which have been the subject of control actions taken in five or
more countries may also be eligible.
14. Once a chemical has been identified
for inclusion in the PIC procedure, a Decision Guidance Document
(DGD) is prepared by FAO/UNEP and sent to each participating country
(through the DNAs) together with an Importing Country Response
form. The DGD provides a summary of toxicological and environmental
characteristics, known usage, possible exposure routes, measures
to reduce exposure and regulatory actions taken by some countries
to ban or severely restrict the chemical, with corresponding reasons
for their actions. The DGD is intended to help Governments assess
the risks connected with the handling and use of the chemical
and to make more informed decisions about future import and use
taking into account local conditions. The DNA then completes an
Importing Country Response form indicating whether to accept import,
refuse import or allow import under certain conditions. The response
is sent to the FAO/UNEP Secretariat who summarize the import decisions
and circulate these to DNAs every six months.[28]
Governments of exporting countries shall, upon receipt of importing
countries decisions, transmit them to their industry. In addition,
this information is also included in the regular updates of the
Consolidated List of Products whose Consumption and/or Sale have
been Banned, Withdrawn or Severely Restricted.
15. The aim of the PIC procedure is to ensure
that a banned or severely restricted chemical is not exported
without the consent of the importing country. The Guidelines require
that if an export is planned of a chemical banned or severely
restricted in the exporting State, then the exporting State should
ensure that the DNA of the importing State is provided with relevant
information to remind the importing State of the original notification
by the exporting State of control action and to alert it to the
fact that an export is planned. The minimum information to be
provided is a copy of the information provided at the time of
notification of the control action, the indication that an export
of the chemical will occur and an estimate of the quantity to
be exported annually as well as any shipment-specific information
that might be available. Such information is to be provided to
the State of final destination and to UNEP/IRPTC. It is also clear
that the PIC procedure is applied to chemicals that have multiple
use. For example, the six monthly PIC circular[29]
of import decisions for some chemicals has in the column headed
"Final Decision on Import" the words "Prohibit
for plant protection use" and then in the column headed "Conditions
for Import" has the words "For uses other than plant
protection, written authorization is required for import."
16. The banned and severely restricted chemicals
thus far subject to the PIC procedure are pesticides and industrial
chemicals; some 27 chemicals or groups of chemicals are already
the subject of DGDs[30]
In some cases, a specific chemical is the subject of a DGD such
as fluoroacetamide, parathion or ethylene oxide, whilst other
DGDs apply to a group of chemicals such as mercury compounds and
polychlorinated biphenyls (PCB), except mono- and dichlorinated.
EU Regulation
17. In the European Union, a legally binding
Council Regulation (EEC) No 2455/92 was adopted[31]
in 1992 which requires exporters of chemicals which are banned
or severely restricted in the European Union to provide information
to importing countries about these chemicals. This regulation
implements the UNEP/FAO PIC scheme in the EU. Member Governments
of the EU are legally required, as well as formally committed,
to implement EEC Regulations. Consequently it is a legal requirement
for an exporter to provide the designated national authority of
the Member State in which he is located with information about
the export from the Community to a third country for the first
time of a chemical subject to the Regulation no later than 30
days before the export is due to take place. The designated national
authority has then to ensure that the appropriate authorities
of the country of designation receive notification at least 15
days before export; copies of the notification are to be copied
to the Commission which shall forward it to the designated national
authorities of the other Member States and to UNEP/IRPTC. The
notification provides information about the identity of the chemical,
information on precautions to be taken, summary of the regulatory
restrictions and the reasons for them, the expected date of first
export, country of designation, use category (whether plant protection
product, industrial chemical or consumer chemical) and the estimated
amount of the chemical to be exported to the destination country
in the next year. The regulation requires the exporter to comply
with the decision of the country of destination participating
in the PIC procedure.
The Rio Summit
18. The United Nations Conference on Environment
and Development held in Rio de Janeiro from 3 to 14 June 1992
(the Earth Summit) reaffirmed the Declaration of the United Nations
Conference on the Human Environment adopted at Stockholm on 16
June 1972 and "working towards international agreements which
respect the interests of all and protect the integrity of the
global environmental and developmental system, recognizing the
integral and interdependent nature of the Earth, our home,"
proclaimed a set of Principles.[32]
Several of these related to the protection of the environment:
19. These Principles are amplified in a
series of Chapters and programme areas; for each the bases for
action, objectives, activities and means of implementation are
addressed. These include:
Within these chapters there are areas addressing
the protection of people and the environment such as:
20. Of particular interest, are various
sections of Chapter 19 (Prevention of illegal international traffic
in toxic and dangerous products). Thus Section C on information
exchange has the objectives of promoting intensified exchange
of information on chemical safety, use and emissions among all
involved parties and of achieving "by the year 2000, as feasible,
full participation in and implementation of the PIC procedure,
including possible mandatory applications through legally binding
instruments." Section F notes that there is currently no
global international agreement on traffic in toxic and dangerous
products (toxic and dangerous products are those that are banned,
severely restricted, withdrawn or not approved for use or sale
by Governments to protect public health and the environment. However,
it was noted that there was international concern that illegal
international traffic in these products is detrimental to public
health and the environment, particularly in developing countries
as acknowledged by the General Assembly in resolutions 42/183
and 44/226.[33]
It went on to say that further strengthening of international
and regional co-operation is needed to prevent illegal transboundary
movement of toxic and dangerous products. The following activities
are detailed:
(a) Adopt, where necessary, and implement legislation
to prevent the illegal import and export of toxic and dangerous
products.
(b) Develop appropriate national enforcement
programmes to monitor compliance with such legislation, and detect
and deter violations through appropriate penalties.
A legally binding PIC procedure
21. The UNEP Governing Council at its meeting
in May 1991 adopted[34]
resolution 16/35 on Toxic Chemicals requesting further urgent
action to be taken to strengthen the legal basis of the amended
London Guidelines taking into consideration experience gained
in the implementation of the Guidelines and PIC procedure. At
the UNEP meeting in May 1995, resolution 18/12 was adopted[35]
to develop an internationally legally binding instrument for the
application of the PIC procedure. This resolution followed consideration
of a report[36]
by the Executive Director of UNEP which noted that one of the
objectives of programme area C of Chapter 19 of Agenda 21 was
to achieve by 2000 full participation in and implementation of
the PIC procedure, including possible mandatory applications through
legally binding instruments. Resolution 18/12 authorised UNEP
in conjunction with FAO to convene "an intergovernmental
negotiating committee with a mandate to prepare a legally binding
instrument for the application of the prior informed consent procedure
for certain hazardous chemicals in international trade."
The resolution also called for the convening of "a diplomatic
conference for the purpose of adopting and signing an internationally
legally binding instrument for the application of the prior informed
consent procedure for certain hazardous chemicals in international
trade, preferably not later than early 1997."
21. The first meeting of the intergovernmental
negotiating committee for an international legally binding instrument
for the application of the PIC procedure was held[37]
in Brussels in March 1996 under the chairmanship of Ms Rodriguez
of Brazil. This session made rapid progress, agreed quickly on
the rules of procedure, and completed a preliminary review of
a draft outline of the future agreement. A working group chaired
by Mr Rawal of India was established to further clarify which
groups of chemicals may be included in the future agreement. The
second meeting was held in September 1996 in Nairobi, Kenya which
made further progress producing 24 pages of draft Convention text
with most of the articles having been extensively discussed. Whilst
substantial progress was made, further detailed consideration
is needed of various aspects of the instrument. A third meeting
was held in Geneva from 26 to 30 May 1997, a fourth in Rome from
20 to 24 October 1997, a fifth in Brussels from 9 to 14 March
1998 and then the Conference of Plenipotentiaries to adopt the
PIC Convention was held on 10 and 11 September 1998 in Rotterdam,
hosted by the Government of the Netherlands.
Analysis
22. There is thus a regularly updated Consolidated
List of Products Whose Consumption and/or Sale Have Been Banned,
Withdrawn, Severely Restricted or not Approved by Governments
which provides information on the restrictive regulatory decisions
regarding over 600 products. This is complemented by a multilateral
export-import system for hazardous chemicals in international
trade currently involving some 148 countries; countries which
have not yet agreed to participate have been invited to do so.
The system requires that information be provided to an importing
country prior to an export of a potentially hazardous chemical
so that the importing country can decide whether to accept, refuse
or allow under certain conditions the import of the chemical.
The decision of the importing country is communicated to the UNEP/FAO
Secretariat who in turn inform the other participating countries
by means of six monthly updates. Consequently, there is considerable
transparency in the operation of the export-import system which
has been successfully applied to multi-use chemicals for which
one use may be banned. The system functions through Designated
National Authorities in each of the 155 countries. The current
system is voluntary although it is legally binding in the European
Union. An international legally binding instrument was adopted
in 1998 and will enter into force when ratified by 50 States.
HEALTH AND
ENVIRONMENT INITIATIVES
23. The Earth Summit, held in Rio de Janeiro
in June 1992, agreed on a set of principles intended to achieve
sustainable development whilst protecting the environment. These
included a commitment to the environmentally sound management
of biotechnology covering five topics: increasing the availability
of food, feed and renewable raw materials; improving human health;
enhancing the protection of the environment; enhancing safety
and developing international mechanisms for co-operation; and
finally establishing enabling mechanisms for the development and
the environmentally sound application of biotechnology.
24. The penultimate topic specifically
recognises the need for further development of internationally
agreed principles on risk assessment and management of all aspects
of biotechnology. The document agreed in Rio says that "only
when adequate and transparent safety and border-control procedures
are in place will the community at large be able to derive maximum
benefit from, and be in a much better position to accept the potential
benefits and risks of, biotechnology."
The Convention on Biological Diversity
25. The Convention on Biological Diversity
(CBD) opened for signature at the Rio summit, entered into force
in December 1993, and currently has 176 States Partiesthe
notable exception being the United States which has signed but
not ratified the Convention. One article of the Convention explicitly
addresses the international distribution of the benefits of biotechnology,
and includes consideration of its safety and transfer aspects.
It states that "The Parties shall consider the need for and
the modalities of a protocol setting out appropriate procedures,
including, in particular, advance informed agreement, in the field
of the safe transfer, handling and use of any living modified
organism resulting from biotechnology which may have adverse effect
on the conservation and sustainable use of biological diversity."
The implementation of the CBD has been taken forward by the Conferences
of the Parties.
26. The first meeting of the signatories
to the biodiversity convention, held in Nassau, Bahamas, at the
end of 1994, set up an ad hoc group of experts on biosafety to
consider the need for, and possible form of, a protocol setting
out appropriate procedures. These included in particular advance
informed agreement, in the field of safe transfer, handling and
use of any living modified organism resulting from biotechnology
that may have an adverse effect on the conservation and sustainable
user of biological diversity.
27. The second meeting, held in Jakarta
in November 1995, agreed a two track approach. An ad hoc working
group would begin negotiations on a biosafety protocol, aiming
to complete this by 1998. In parallel, efforts would be made to
finalize the United Nations Environmental Programme (UNEP) International
Technical Guidelines on Safety on Biotechnology. These two initiatives
are intended to be complementary, in that the protocol will be
a binding agreement setting out what States must do, while the
UNEP guidelines are intended to indicate how to do it.
28. UNEP's international guidelines on biosafety
were adopted by a meeting of government-designated experts held
in Cairo in December 1995, and were subsequently issued by UNEP.
They have since been developed at a further meeting held in Zimbabwe,
Costa Rica, Thailand, Hungary, the Slovak Republic as well as
in Cartagena, Columbia and Budapest, Hungary.
29. The biosafety working group met for
the first time in July 1996 in Aarhus, Denmark, and has since
held four further meetings in Montreal and a sixth meeting in
Cartagena, Columbia at which the draft biosafety protocol was
further developed. A final meeting was held in Montreal on 24
to 28 January 2000 at which the Cartagena Protocol on Biosafety
was adopted.
The Cartagena Protocol on Biosafety
30. The Cartagena Protocol on Biosafety
address the safe transfer, handling and use of living modified
organisms (LMOs) that may have an adverse effect on biodiversity
with a specific focus on transboundary movement. The Protocol
establishes an Advance Informed Agreement (ALA) procedure for
imports of LMOs which incorporates the precautionary principle.
It also contains provisions regarding confidential information
and information sharing, capacity building and financial resources,
with special attention to developing countries and those without
domestic regulatory systems. The Cartegena Protocol will open
for signature in Nairobi from 15 to 26 May 2000 on the occasion
of the Fifth Session of the Conference of the Parties to the Convention
on Biological Diversity and will enter into force after 50 countries
have ratified it.[38]
Regulatory Frameworks
31. Although the actions stemming from the
Rio Summit have focused world attention on protection of human
health and the environment, many countries have long recognised
the potential threat of dangerous diseases to their people, as
well as to the livestock and crops on which they depend. As a
result, many have introduced national regulations to control the
handling, use, storage and transfer of hazardous pathogens. More
recently, countries have sought to harmonise their national regulations
both regionally and internationally, in order to facilitate co-operation
and trade.
32. Under such regulation, those wishing
to work with pathogenic organisms are usually required to provide
information to national authorities, who frequently carry out
inspections of the facility in which the pathogens are to be handled.
Such notification and inspection can be required prior to any
work being carried out. In addition, transfers of pathogens that
present a particular danger are controlled and monitored in several
countries, while in many countries, there are additional regulations
on the handling and use of genetically modified organisms.
33. There are parallel regulations for the
licensing of facilities engaged in producing medicinal products
for humans and veterinary products for animals to ensure that
the products are safe and effective. These require repeated inspection
of such facilities to ensure that standards for good manufacturing
practice are being met. Such regulations promote trade in pharmaceuticalswhilst
building confidence that such facilities are not being used for
prohibited purposes.
34. The net effect of all these controls
and regulations is to provide a national framework intended to
ensure that the danger presented by pathogens to both public health
and the environment is minimized and that medical products are
safe, and thereby providing assurance to the public in the country
concerned.
35. Increasingly, there are moves to harmoize
such measures both regionally and internationally, in the recognition
that an outbreak of human, animal or plant disease in one country
can easily spread to other countries in a regionor, in
this era of increasing international trade and travel, even more
widelyand to promote trade in safe medicinal products.
There are therefore both regional and international initiatives
to extend national frameworks to regulate dangerous pathogens
into regional and global frameworks, to increase public assurance
that the dangers from disease outbreaks both at home and abroad
have been minimized.
Analysis
36. One objective of international security
is to ensure that the use of diseases as a weapon of war is totally
prohibited, and to devise a regime to monitor compliance with
this prohibition, in order to detect and deter cheaters. The pathogens
that can be used as a weapon of war are precisely those that present
a danger in natural outbreaks of disease. Thus two important elements
of a regime to strengthen the BTWC are for declarations about
facilities and activities of particular relevance to the Convention
to be made to national authorities and to the international organization
and for these declarations to be confirmed by infrequent visits
to ensure that declarations are accurate and complete. These elements
thus closely parallel the requirements in many countries for notification
and inspection of facilities working with dangerous pathogens.
37. These are common goals between the ongoing
negotiation to develop a Protocol to the BTWC in Geneva and Biosafety
Protocol. There are synergistic benefits to be gained, both for
public health and environmental safety and for international security,
through the regime to strengthen the BTWC building upon the controls
and regulations for public health and environmental safety and
seeking to harmonise and strengthen these. This would help capacity
building and also, by building upon existing national authorities
and reporting requirements, reduce the administrative burden and
avoid duplication of effort. The potential benefits for both developed
and developing countries in doing so are both tangible and significant.
OVERVIEW
38. Although it is widely recognised that
microorganisms and their applications through biotechnology offer
immense benefits to the global community, public concern about
microorganisms has grown in recent years. There is a much greater
and widespread awareness of the dangers of disease whether Ebola
outbreaks in Zaire or BSE in cattle and the possible spread to
humans and concerns about the consequences of genetic engineering
such as in modified foodstuffs. In addition, the possibility that
disease may be spread deliberately as a weapon of war or as a
terrorist attack is rightly attracting much attention.
39. Similarly, chemicals are also rightly
seen as bringing potential benefits to the global community, although
there has been increasing concern about the potential harmful
side-effects of some chemicals and pesticides. This has led to
concern in both developing and developed countries that such chemicals
should be assessed and evaluated to ensure that they do have damaging
effects on health or the environment. In addition, the possibility
that chemicals may be used to attack humans or animals as a weapon
of war or as a terrorist attack has received much attention since
the use of chemical weapons in the Iraq-Iran war of the 1980s
and the Aum Shinrikyo attack on the Tokyo subway in March 1995.
40. As in all these instances the concerns
stem from the ways in which microorganisms and chemicals are used,
stored and transferred, there is a common goal in the initiatives
being taken to protect human health and environmental safety,
following the Earth Summit and for biological materials, the Convention
of Biological Diversity (CBD) and the recent agreement on 29 January
2000 of the Cartagena Protocol on Biosafety, and to ensure that
disease is not being used as a weapon of war to cause harm to
humans, animals and plants through strengthening of the Biological
and Toxin Weapons Convention by a Protocol. Insofar as chemicals
are concerned, there is a similar common goal between the initiatives
being taken to protect human health and the environment from certain
hazardous chemicals following the Earth Summit and the adoption
in September 1998 of the Rotterdam Convention on the Prior Informed
Consent procedure, and to ensure that chemicals are not used as
a weapon of war by the Chemical Weapons Convention which entered
into force in April 1997.
42. The synergy between these objectives
needs to be harnessed for the benefit of all. Achievement of a
safer, more prosperous world is indeed a challenge. In considering
this, it is useful to consider graphically the developments in
both security and health and environment regimes:
43. Consideration together of both security
regimes and health and environment regimes bridges the gap between
developed and developing countriesand can bring benefits
to both through a recognition of the common goals of these regimes.
Both the CWC and the BTWC have Articles that promote international
collaboration for peaceful purposes in regard to chemical and
microbial agents and toxins respectively. During the negotiation
of the Protocol to strengthen the BTWC, the contributions to transparency
and to building confidence in an integrated regime have increasingly
been recognised[39]
and language in the draft Protocol requires States Parties to
promote and support a range of activities relating to the peaceful
uses of microbiology and biotechnology including the surveillance
and treatment of infectious diseases.
CONCLUSIONS
44. The Foreign Affairs Committee is recommended
to :
18
FAO/UNEP Joint Programme for the Operation of Prior Informed Consent,
Prior Informed Consent, Update on Implementation as of 30 June
1998. Available at http://irptc.unep.ch/pic/volpic/english/UPDATEN9.html. Back
19
Council Regulation (EEC) No 2455/92 of 23 July 1992 concerning
the import and export of certain dangerous chemicals, Official
Journal of the European Communities, L251, Volume 35, 29 August
1992, pp 13-22. See also European Chemicals Bureau, Informing
the Importer, Guide to Council Regulation (EEC) No 2455/92 concerning
the import and export of certain dangerous chemicals, 1996. Back
20
United Nations Environment Programme, Governing Council decisions
85(V), 25 May 1977. Back
21
United Nations General Assembly, Resolution 37/137, Protection
against Products Harmful to Health and the Environment, 109th
Plenary Meeting, 17 December 1982. Back
22
United Nations Department of International Economic and Social
Affairs, Consolidated List of Products whose Consumption and/or
Sale Have Been Banned, Withdrawn, Severely Restricted or not Approved
by Governments, Fourth Edition, United Nations, New York,
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