Annexes to COM(2002)27 - Life sciences and biotechnology - A Strategy for Europe - Main contents
Please note
This page contains a limited version of this dossier in the EU Monitor.
| dossier | COM(2002)27 - Life sciences and biotechnology - A Strategy for Europe. |
|---|---|
| document | COM(2002)27  |
| date | January 23, 2002 |
Dialogue should be open for all stakeholders. Public authorities should help to ensure participation by stakeholders with limited resources. Economic operators, industry and users, who have economic interests at stake, as well as the scientific community, bear a particular responsibility for active participation. The Commission invites these parties to respond to public concerns, for example through transparency of their visions, policies and ethical standards.
Relevant public information is essential for meaningful dialogue. Providing it requires focused and pro-active efforts. It is especially important that the information needs formulated by the broad public are taken seriously and responded to. We shall also strive for a balanced and rational approach, distinguishing between real issues, on which we must act, and false claims.
4.2. Developing life sciences and biotechnology in harmony with ethical values and societal goals
Without broad public acceptance and support, the development and use of life sciences and biotechnology in Europe will be contentious, benefits will be delayed and competitiveness will be likely to suffer.
The debate and the public consultation carried out by the Commission [6] indicate that the European public is quite prepared and capable to enter into complex weighting of benefits against disadvantages, guided by fundamental values. Although sometimes polarised, the public debate demonstrates many points of converging views.
[6] The Commission intends to publish these comments on the Internet
Public opinion depends crucially on the perceived benefits of life sciences and biotechnology. Eurobarometer surveys reveal that public expectations of biotechnology, apart from medical advances, are moderate. And there is also considerable public uncertainty about some applications, and aversion towards their distributional impacts and the risks involved.
There is broad support for many guiding values and goals. Some of these, such as the freedom of research, intrinsic value of new knowledge and the moral obligations to help alleviate illness or hunger, tend to favour the development and application of these new technologies. Others help to clarify the criteria and conditions for the development and applications of life sciences and biotechnology, in particular the need to take into account the ethical and societal implications, and the importance of transparency and accountability in decision-making, minimising risk, and freedom of choice.
It is therefore of key importance to support information and dialogue to help the public and stakeholders better understand and appreciate these complex issues and to develop methods and criteria for assessing benefits against disadvantages or risks, including the distribution of impacts among different parts of society.
Our democratic societies should offer the necessary safeguards to ensure that the development and application of life sciences and biotechnology take place respecting the fundamental values recognised by the EU in the Charter of Fundamental Rights, in particular by confirming the respect for human life and dignity. The Community has also banned funding of research into human reproductive cloning. Support should be given to the Frano-German initiative, addressed to the UN, for a world-wide convention on the prohibition of human reproductive cloning. Other issues such as stem cell research clearly require attention and further debate. Europe has also taken clear positions on the importance of freedom of choice for consumers as well as for economic operators with respect to GM foods, and we have established broad societal agreement on the need to safeguard European agricultural practices.
However, scientific and technological progress will continue to give rise to new ethical or societal implications. The Commission considers that these issues should be addressed pro-actively and with a broad perspective, taking into account the moral obligations towards present and future generations and the rest of the world. We should not content ourselves with acting defensively only when our core values are being transgressed.
These issues cannot be adequately addressed within the narrow context of regulatory product approvals but require more flexible and forward-looking approaches. Europe needs an active and on-going public dialogue, accompanied by focused fact-finding on both benefits and disadvantages to allow the public to contribute to the complex process of setting priorities. In the context of its Science & Society initiative [7], the Commission has already proposed a series of actions intended to strengthen the ethical dimension in sciences and new technologies.
[7] COM(2001)714 of 4.12.2001
To be at the front of developments, Europe should have the capacity for foresight/prospective analysis and the necessary expertise to help clarify the often complex issues for policy makers and the public, and to place them in their scientific and socio-economic context. The Commission welcomes the key role played by the European Group on Ethics in Science and New Technologies since its creation in the early 1990s and proposes, as part of the present strategy, to enhance its role and to reinforce the networking with and between national ethical bodies. To this end, an additional targeted consultation of the other Community institutions is envisaged.
Moreover, transparency, accountability and participatory approaches in public policy-making need to be reinforced. These objectives coincide with those of the Commission's White Paper on European Governance [8] and will be pursued through the actions proposed therein.
[8] COM(2001)428 final of 25.7.2001
4.3. Demand-driven applications through informed choice
The regulatory oversight applied to the development and use of life sciences and biotechnology is the expression of societal choices. Regulation and other public policy measures set the rules and conditions, under which life sciences and biotechnology may be developed and applied. Regulation should therefore ensure that market mechanisms function effectively to obtain the stated objectives. This is the purpose of Europe's policy of mandatory labelling which aims to ensure that consumer's preferences are translated into incentives for producers to adapt supply.
As far back as 1990 and after lengthy discussions, the Community opted for a science-based regulatory approach that subjects all commercial uses of genetically modified organisms to ex-ante public scrutiny and safety approval on a case-by-case basis, prior to any application, release into the environment or marketing. As a result of this approach, a revised framework legislation on GMOs has been adopted and will enter into force in October 2002. The new legislation provides a sound basis to overcome the present standstill in authorising new products.
* Under the Community's regulatory approach in sectors where pre-marketing authorisation is required, authorisation is granted after a scientific evaluation of the risks which the product may present for human and animal health or for the environment, taking into account other factors legitimate to the matter under consideration. In the logic of this approach, it is for the markets to determine whether products survive. But it is essential to ensure that the market mechanisms work effectively so that consumers can exercise choice and thus send clear signals to suppliers. Over the last 5 years, Europe has pioneered solutions to ensure informed consumer choice through labelling - these need urgently to be completed and put into application.
* In order to fully apply the principle of freedom of choice for economic operators and to safeguard sustainability and diversity of agriculture in Europe, public authorities in partnership with farmers and other private operators need to develop agronomical and other measures to facilitate the co-existence of different agricultural practices without excluding GM crops.
4.4. Confidence in science-based regulatory oversight
Where safety is an issue, Community legislation is science-based and its application with respect to specific decisions will be in accordance with the precautionary principle [9]. The European Agency for Evaluation of Medicinal Products is a successful example of setting high standards of scientific advice and effective risk communication. With the creation of the European Food Safety Authority (EFSA), the already high standards of excellence, independence and transparency of scientific advice in that field will be taken further and new emphasis will be placed on risk communication. EFSA will be responsible for scientific assessments of environmental, human and animal health effects of GMOs and GM food and feed, and will have a forward-looking responsibility for identifying emerging risks, including those potentially arising from the application of biotechnology in agri-food production. These are essential contributions to public trust in the scientific basis for regulatory oversight for the safety of existing foods and medicines as well as new applications. Building public confidence and understanding must be a permanent concern.
[9] Commission's Communication on the Precautionary Principle COM (2000)1 final of 2.2.2000, and the Nice European Concil conclusions
* There is a general need to enhance public trust in the role of science in our societies. The Commission has proposed an action plan on Science & Society to promote scientific culture, to better take into account public needs in setting the scientific agenda, and to place science at the heart of European policies. Public authorities, economic operators and the scientific community should actively present relevant knowledge and facilitate understanding on key issues, including that scientific knowledge is always advancing and therefore regularly improves our reference points. Moreover, it is an essential part of the process of public understanding and policy formulation to also evaluate the risks of not taking action, for example against the evolution of new or drug-resistant diseases and in areas where current agricultural practices are unsustainable.
* Biotechnological inventions require high capital investment, long development cycles and comprehensive regulatory approval. Effective patent protection is a crucial incentive to R&D and innovation and an essential means of guaranteeing return on investment. Moreover, the disclosure of information in patent publication has been important in contributing to the overall development of biotechnology. In view of the rapid scientific progress, legislation on intellectual property needs to be monitored very closely. Regular assessments need to be made on whether the patent regime satisfies the needs of researchers and companies. In this respect, the EC and its Member States should ensure that the interpretation of the essential criteria of novelty, invention and utility in the field of life sciences is not left exclusively to courts and patent offices. As regards the international context, there is a need to work towards a level playing field in patent protection in industrialised countries. Steps need to be taken in view of promoting international dialogue on this issue.
* The basis for Community regulation of these new technologies should be more transparent and better communicated. For example, we should be clearer about how regulators deal with risk - potential risk, scientific uncertainty (e.g. the absence of zero-risk, the application of the precautionary principle), weighing of comparative risks, the role of the different stages of risk analysis, the role of risk management measures such as monitoring and safeguards, and their proportionality with risk. In addition, whilst underlining the importance of legal certainty and predictability, we need to stress the reversibility of regulatory decisions when justified and highlight the on-going work on international convergence of risk analysis methodologies and development of anticipatory risk analysis methodologies. Publicly funded research in support of regulatory oversight is of particular importance for public confidence.
* Specific initiatives proposed in the Commission's White Paper on European Governance are particularly relevant for enhancing public confidence, in particular the planned improvements for openness and accountability in risk governance and in use of expertise.
* Confidence in our regulatory oversight is a responsibility of public authorities but also requires the responsible participation of other stakeholders such as the biotechnology industry, other economic operators, the scientific community, NGOs and the media.
4.5. Regulatory principles
Community regulation currently governs such diverse aspects such as the patenting of biotechnological inventions, the authorisation of pharmaceutical products, contained use of genetically modified microorganisms, and release and marketing of products consisting of or derived from GMOs, including foods, feeds and seeds. This regulatory framework has evolved gradually over the last 25 years, with major developments in recent years.
In order to improve the coherence, transparency and efficiency of Community regulation, the Commission suggests that Community regulatory activity should respect the following principles:
* Risk governance and product authorisation: Products of biotechnology should, in accordance with the established regulatory principles and frameworks, be authorised on the basis of a comprehensive scientific risk assessment if found to be safe for human, animal or plant life and health and the environment. In cases where scientific evidence is insufficient, inconclusive or uncertain, and where possible risks are judged to be unacceptable, risk management measures should be based on the precautionary principle. Risk management should take into account the results of risk assessment and other factors legitimate to the matter under consideration in order to achieve the chosen level of protection.. Procedures for authorisation should be transparent, risk assessments should be published and made available for public comment as part of the authorisation procedures. Communication needs to be an integral part of risk assessment and risk management activity.
* Safeguarding the Internal Market: To secure the functioning of the Internal Market and legal certainty, Community legislation should be drafted and periodically reviewed to ensure coherence and efficiency, including with regard to its practical feasibility and enforceability. Implementation of and compliance with Community law should be carefully monitored, and any problem of compliance should be addressed and resolved among concerned parties according to existing procedures in a transparent and predictable manner.
* Proportionality and consumer choice: Community regulatory requirements should be proportionate to the degree of identified risk and should conform with the Community's international obligations. As proposed by the Commission, Community legislation should facilitate consumer choice through ensuring that consumers/users are informed in cases where a food, feed or seed is genetically modified or derived from GMOs.
* Predictability, modernisation and impact assessment: The Commission should periodically publish a rolling regulatory work programme (see point 6 below) to improve predictability, transparency and quality of regulation. Regulation should continue to be regularly reviewed to be up-to-date with scientific and technological progress, for evaluation of impacts and for conformity with the present principles.
5. Europe in the world - responding to global challenges
The revolution in life sciences and biotechnology is global. Research is fundamentally international - knowledge and experts circulate throughout the world. A growing number of countries are actively pursuing biotechnologies, and the resulting products and services will increasingly be traded on global markets, with a premium for first innovators.
It is also clear that great diversity exists between countries and regions with respect to their capacities to develop, regulate and apply the new products and services. Even greater diversity may emerge with respect to the priorities and societal values that will shape the approaches and choices to developing and using these new technologies.
European policies should not be developed in isolation. We need to embrace the wider international context which shapes both challenges and opportunities for Europe, and we must respond with responsible and proactive policies at the global level. A main objective must be to ensure that the EU maintains competitiveness vis-à-vis major industrialised countries such as the US and Japan. Moreover, whatever policies Europe will decide regarding life sciences and biotechnology, they will have important international impacts, in particular for developing countries. The interests of these countries must also be taken into account. We must integrate the international dimension into all relevant policies, and we need to develop an international agenda, based on our fundamental values and long-term objectives, to actively promote balanced and responsible policies globally, in particular towards the developing world.
5.1. A European agenda for international collaboration
International collaboration is required to manage the novel issues raised by life sciences and biotechnology and the diversity of capacities and policies in different countries and regions towards their applications.
Trade in goods and services is already being affected due to divergent product approval rates. International trade friction may also emerge if countries and regions adopt divergent regulatory frameworks. There is a need for international dialogue on regulatory issues to develop mutual understanding of basic principles and values underlying regulatory developments in different countries.
The Community is committed to open, multilateral, and rules-based trading systems. We should therefore promote respect and implementation of existing international agreements. Given the particular issues raised by life sciences and biotechnology, the Community should promote solutions and dialogue at international level that:
* Ensure mutual supportiveness between relevant international agreements and in particular between the WTO agreements and the Biosafety Protocol.
* Support a coherent, comprehensive, effective, transparent and inclusive approach to biotechnology across the relevant international fora in order to avoid overlaps and make the best use of their respective expertise (including FAO, UNEP, CBD, WTO, WHO and UNCTAD [10]). Europe should continue to play a full part, in particular in the OECD and the Codex Alimentarius, and notably its Ad Hoc Intergovernmental Task-Force on Biotechnology, to promote within these organisations the development and periodic review of harmonised guidelines with respect to the risk analysis, the labelling and the traceability of products derived from modern biotechnology. The role and efficiency of EU participation in international discussions should be enhanced, including through discussions with developed and developing countries. Dialogue should promote mutual understanding of concerns and objectives of different countries and regions, such as the EU/US Biotechnology Forum which delivered its final report in December 2000 [11]. Early policy dialogue about forthcoming legislation may reduce the potential for international friction.
[10] Food and Agriculture Organisation, United Nations Environmental Programme, Convention on Biological Diversity, World Trade Organisation, World Health Organisation, United Nations Convention on Trade and Development
[11] http://europa.eu.int/comm/external_relations/us/biotech/biotech.htm
5.2. Europe's responsibilities towards the developing world
Life sciences and biotechnology hold the promise of meeting some of the fundamental needs for food and health facing the developing world. The UNDP, in its 2001 Human Development Report, highlights the potential of biotechnology for the developing world [12]. Some emerging economies such as China, India and Mexico have already initiated ambitious national development programmes.
[12] http://www.undp.org/hdr2001/
Life sciences and biotechnology are not a panacea and will not resolve the distributional problems of the developing world - but they will be one of the important tools. New capacities should help developing countries reconcile yield increases, sustainable use of natural resources, economic efficiency and social acceptability. Potential applications must be adequately researched and assessed, taking full account of both the environmental safety issues and the needs expressed by the populations concerned to reduce poverty and strengthen food security and nutritional quality.
As a major actor in life sciences and technologies, Europe has a particular responsibility to help the developing world deal with the risks, challenges and opportunities, and to facilitate the safe and orderly development of these technologies at the global level. Europe already holds an influential position in international deliberations on life sciences and biotechnology. This needs to be taken forward with responsible policies to achieve our strategic objectives and to allow the safe and efficient use of life sciences and biotechnology in developing countries.
* Europe should continue to promote protection of biodiversity and the implementation of the Biosafety Protocol for international trade in living modified organisms. Moreover, Europe should continue to support negotiated multilateral frameworks such as the Convention on Biological Diversity and the FAO International Undertaking on Plant Genetic Resources. These international instruments regulate access to genetic resources and the sharing of the benefits arising from their use, in view of providing compensation to the centres of origin of genetic resources and the holders of traditional knowledge used in biotechnological inventions. The EC should contribute to ensure that the benefits generated by biotechnological inventions, including intellectual property income, are properly shared with the providers of genetic resources or traditional knowledge.
* Europe should contribute to technical assistance, capacity-building and technology transfer to allow developing countries to participate in negotiating and implementing international agreements and standards, notably on risk governance, and to safely develop and apply these new technologies if they so wish. Europe should support local initiatives for dialogue on biotechnology among public and private stakeholders and civil society in partner countries.
* Europe should encourage equitable and balanced North-South partnerships and public research for demand-driven applications of life sciences and biotechnology.
* Domestic European policies with regard to life sciences and biotechnology are bound to have major impacts on developing countries. Whilst not compromising EU food safety requirements or consumer information policies, we should provide technical assistance and capacity building to ensure that our policies do not, unwittingly, prevent developing countries from harvesting desired benefits. In particular, we should guard against regulatory requirements that may be manageable only in the industrial world but are unachievable by developing countries, thereby either upsetting existing trade or effectively blocking developing countries from developing life sciences and biotechnology at their own wish and pace.
6. Implementation and coherence across policies, sectors and actors
Europe does not have a single policy for life sciences and biotechnology but a patch-work of specific regulation, overlaid by many sectoral and horizontal policies at international, Community, Member State and local levels. If, with so many actors and policies involved, Europe is to successfully manage life sciences and biotechnology and reap the benefits for society, we should proceed on the basis of a shared vision for a co-operative approach and with effective implementing mechanisms to compensate for absence of overall responsibility and control. Without such mechanisms, life sciences and biotechnology risk to continue to suffer indecision or short-sighted and local solutions.
The Commission proposes to structure and support implementation of the present strategy and the enclosed action plan through the following measures:
* To monitor progress in policy development and on the ground, and to anticipate emerging issues in this fast-developing area, the Commission will, starting in 2002 and ending in 2010, present a regular Life Science and Biotechnology Report, including a rolling work programme for legislation.
* We need to ensure coherence across Community legislation and policies directly regulating, or indirectly impacting on, the development and application of life sciences and biotechnology. The Commission will, as part of its Life Science and Biotechnology Reports, review the coherence of Community policies and legislation affecting life sciences and biotechnology and launch initiatives and proposals as appropriate. Particular attention will be given to ensure that regulation on life sciences and biotechnology adequately integrates our international objectives and facilitates innovation and international competitiveness, that Community research contributes coherently and effectively to Community objectives, and that other Community policies and objectives (e.g. in environment, public health and consumer protection, education, employment, agriculture, trade and development policies) adequately reflect the long-term and global importance of life sciences and biotechnology. The Commission will evaluate whether existing international fora and bilateral dialogues are sufficiently effective and provide adequate flow of information, and whether the domestic coordination mechanisms can be improved.
* Where different levels of competence apply, the strategy should be a reference for collaboration between different actors (Community, national and local public authorities, economic operators, the scientific community etc). As part of the Lisbon strategy, coherent action for life sciences and biotechnology should be pursued through the established methods of coordination and benchmarking. In addition, new forms of collaboration and partnerships between stakeholders should be encouraged. Together with Member States, the Commission will also assess whether current patterns of competence and mechanisms of co-operation allow the effective achievement of the strategic objectives, incl. reassess whether there is a need for reinforcing Community competence in accordance with the Treaty.
* The Commission invites all institutions and public actors to strive for better coherence in their action. For its own part, it will seek to provide the vigilance and political impetus to keep momentum in implementing the present strategy, through its own action or through recommendations and invitations to other parties. The Commission intends to hold more regular orientation debates, coinciding with the adoption of the above mentioned Commission Life Science and Biotechnology Report.
* In order to facilitate transparency and structured dialogue on the further development and implementation of the proposed strategy for life sciences and biotechnology, the Commission will organise a broadly based Stakeholders' Forum, including representatives of the candidate countries and third countries.
7. A framework for dialogue and action
It is time to clarify the strategic opportunities and challenges facing Europe. Life sciences and biotechnology are a global reality and essential for the objective of developing dynamic and innovative knowledge-based economies. We have to face the difficult questions and identify our strategic objectives to avoid the pitfalls of short-term solutions to long-term challenges and of local solutions to global challenges.
Recognising that life sciences and biotechnology raise particular challenges, the Commission undertook to propose a strategy and concrete actions. It now presents this initiative for a coherent, collaborative and sustained effort.
The present initiative draws on a thorough analysis [13] of the strengths and weaknesses of European biotechnology, and a broad public debate and the specific public consultation launched by the Commission in September 2001. The initiative should, in turn, itself inspire further dialogue. The attached action plan suggests a broad scope of measures according to the orientations set out in chapters 3 to 6 of this Communication. It constitutes a framework, within which some actions can be launched in the short-term while other actions for the medium and longer term are identified and suggested for further development in collaboration with Member States and stakeholders.
[13] European Competitiveness Report 2001, Luxembourg 2001; "Innovation and Competitiveness in European biotechnology", Enterprise Papers - N° 7, 2002, European Commission
The Commission now invites the Community institutions and bodies, the Member States, protagonists and the public to contribute to refine and implement the proposed strategy by defining detailed measures under both short- and medium-term actions and the time-plan for their deliverables, as a first decisive step towards an effective and coherent European biotechnology policy.
* *
Life sciences and biotechnology - A strategy for Europe
PART II: ACTION PLAN
1. HARVESTING THE POTENTIAL
The resource base
Investing in People
Action 1
The Commission will together with competent authorities in Member States [14] identify the education needs in life sciences within the 10-year Objectives for Learning in the Knowledge Society [15] and:
[14] Where reference is being made to the Member States in the action plan, the Commission will examine with interested candidate countries their participation.
[15] Education Council Report to the European Council 5980/01
a) strengthen a broad education and understanding of life sciences,
b) develop and train a skilled workforce in life sciences,
by issuing recommendations for curricula and teacher training. Community support can be provided under the Comenius and Erasmus programmes.
c) As set out in its Communication on the European area of Lifelong learning [16], the Commission will work with Member States, industry, academia and others to identify measures to promote continuing education and refresh the current competence of the scientific workforce. Community support can be provided under the Leonardo programme.
[16] COM(2001) 678
d) The Commission and Member States should support discussion fora for specialist scientists, with the objective of stimulating an exchange across disciplines. Vital discoveries frequently happen at the point where disciplines intersect. Community support can be provided under the Erasmus programme.
Implementer: Member States, Commission, private sector
Timeframe: 2003-2010
Action 2
The Commission will explore with Member States
a) the opportunity and best way to establish efficient methods to match a skilled workforce with job opportunities, involving effective communication of open positions, collaboration with established companies and a labour force aware of available employment options.
b) possible measures to attract and retain scientists and avoid brain drain. In achieving this, specific reference will be paid to the initiatives launched under the Communication « A Mobility Strategy for the Research Area" [17], which aims at improving the overall environment of researchers and their families in the EU. Due attention will also be paid to the increased mobility opportunities offered by the forthcoming Sixth Framework Programme (2002-2006), and more particularly to the measures aimed at attracting foreign researchers and supporting the return of EU researchers established in other parts of the world.
[17] COM(2001)331final, of 20 June 2001,as supplemented by the Council's Resolution of 20 December 2001 concerning « The Reinforcement of the Mobility Strategy within the European Research Area ».
Implementer: Member States, Commission
Timeframe: 2003 onwards
Generating and exploiting knowledge
Research
Action 3
The Commission will enhance its support for life sciences and biotechnology research, technological development, demonstration and training activities under the next Framework Programme 2002-2006 aimed at contributing towards the creation of the European Research Area.
Biotechnology research will be supported under the thematic priorities, including:
1: Genomics and biotechnology for health
3: Nanotechnologies
5: Food quality and safety
6: Sustainable development
7: Citizens and governance
Specific measures will be provided to encourage SME participation, international cooperation and mobility and training of researchers.
The new instruments of Networks of Excellence and Integrated Projects will facilitate the objectives of Europe-wide collaborations, attaining critical mass and simplification of administrative procedures.
The Commission and the Member States should also in collaboration with the European Investment Fund (EIF) develop a competitive bioinformatics infrastructure in support of biotechnology research and focus support for the development of research in computational biology and bio-medical informatics.
Implementer: Member States, EIF, Commission
Timeframe: 2002-2006
Management and legal services
Action 4
Enhancing the supply of specific management and legal skills:
a) Member States and national biotechnology associations should examine the opportunity of creating self-sustained networks of biotechnology company managers at the national level.
b) Member States and the Commission should promote collaboration between law schools, law firms and companies for the development of specific legal competence needed by biotechnology companies.
Implementer: Member States, academia, professional associations, Commission
Timeframe: 2003 onwards
Exploitation of intellectual property
Action 5
A strong, harmonised and affordable European intellectual property protection system, functioning as an incentive to R&D and innovation will be finalised by:
a) Member States urgently transposing into national laws the Directive on the Legal Protection of Biotechnological Inventions EC/98/44.
b) Council adopting the Community Patent Regulation.
c) Member States and the Commission clarifying rules on ownership of intellectual property stemming from public research and monitoring the effect of implementation of patent legislation on research and innovation.
d) encouraging awareness training in the strategic use of IPR during the entire research and innovation process and raising awareness among academics of the commercial potential of their research, encouraging entrepreneurship and movement between academia and companies.
e) taking steps to promote international dialogue and co-operation with a view to work towards a level playing field with industrialised countries in patent protection on biotechnology inventions, ensuring an effective level of protection for innovation in this field.
Implementer: Member States, Council, Commission
Timeframe: 2002 onward
Capital base
Action 6
The Commission should together with the European Investment Bank (EIB) and the European Investment fund (EIF) strengthen the capital base for the biotechnology industry, by:
a) seeking to stimulate investments in research and technological innovation via complementary financing on the basis of the co-operation agreement signed in June 2001 between the Commission and the EIB group.
b) seeking to stimulate investments in business incubators through the EIF Start Up Facility
c) studying measures to support technology transfer mechanisms, such as financing of patent pools or other methods for patent exploitation.
d) studying measures to encourage commercial financing of companies based on a medium-term investment perspective.
Implementer: EIB Group, Commission
Timeframe: 2002 onwards
Action 7
The Commission will strengthen the work of the Biotechnology and Finance Forum by the inclusion of relevant major stakeholders to provide advice into policy development in the field of capital supply.
Implementer: Commission
Timeframe: 2002
Networking Europe's biotechnology communities
Networks in Europe
Action 8
The Commission will:
a) support creation of a commercial biotechnology web portal for Europe that will help free access to information and networking available Internet platforms. The contents of such a portal will have to be defined based on the requirement of economic viability and sustained demand.
b) develop its newly created Commission web site to provide a broad entry platform into the Commission's work on biotechnology.
Implementer: Commission
Timeframe: 2002-2003
Action 9
Member States, their regions, the Commission and EIB should support:
a) stronger interregional co-operation, e.g. through a network of biotechnology regions. Crossborder and interregional co-operation can receive funding from the Interreg programmes (notably Interreg IIIB and IIIC).
b) networks of biotechnology clusters. In addition, the Commission will organise a European competition between Biotechnology Innovation clusters, to highlight their capability to develop a cluster with a focus of excellence in a specific scientific field.
Implementer: Member States, Regions, EIB, Commission
Timeframe: 2003-2006
A proactive role for public authorities
Action 10
The Commission will establish
a) a competitiveness monitoring function and a contact network with Member States ministries with responsibility for competitiveness in biotechnology. Monitoring should include impact on European competitiveness of legislation and policy measures.
b) a Competitiveness in Biotechnology advisory group with industry and academia to assist in identification of issues affecting European competitiveness. The Group will provide input into the Commission's regular reports on Life Sciences and Biotechnology.
Implementer: Member States, Commission
Timeframe: 2002
Action 11
Transparency in the administrative process:
a) The Commission and Member States ,as regulatory authorities, should aid applicants, especially from start-up companies and SME's, requesting approval through the regulatory process.
b) The Commission will issue a guide to Community regulation for users and for entrepreneurs who have limited staff and expertise in the regulatory and legal fields. Such a guide should also benefit non-EU (e.g. developing world) applicants and the general public.
Implementer: a) Member States, Commission. b) Commission
Timeframe: 2003 onwards
Action 12
In collaboration with the involved actors, the Commission will benchmark good practices in clustering biotech companies and in the work of business incubators and disseminate results. The Commission will also establish with Member States a programme for benchmarking relevant elements of biotechnology policies, in addition to existing benchmarking structures.
Implementer: Commission
Timeframe: 2003 onwards
2. A key element for responsible policy: governing life sciences and biotechnology
Societal scrutiny and dialogue
Action 13
The Commission, Member States, organisations, institutions and other actors should engage in a structured dialogue at various levels to develop an understanding and information exchange on life sciences and biotechnology. The Commission will in particular help mobilise all key actors in the public debate and facilitate participation of stakeholders with limited resources.
In particular:
a) The Commission will propose a framework for a process of dialogue and follow-up with stakeholders as a result of the European strategy for life sciences and biotechnology. The framework will notably include a broadly based Stakeholders' Forum. In this process, the Commission will take the initiative to better explain Europe's regulatory approach (including the application of the precautionary principle, the role of risk management, monitoring, safeguards and reversibility of regulatory decisions).
b) The Commission will take initiatives, and invites the scientific community and other stakeholders to assist, to promote awareness of key scientific paradigms underlying regulatory oversight such as scientific uncertainty, absence of zero risk, comparative risks, that science is continuously evolving and therefore continuously improves our reference points, and the articulation between the steps in the risk analysis process. Within their respective fields, the European Food Safety Authority and the European Agency for the Evaluation of Medicinal Products will play an important role in general risk communication, including the scientific background for their conclusions of risk assessments.
c) Beyond these two specific initiatives, the Commission will also encourage public debates on biotechnology between scientists, industry and civil society, including specific interest groups, such as patients groups, farmers and consumers, focussing on specific technological developments, to raise public interest in such developments and offer early information on potential benefits and risks. Developers in the scientific community and in industry have a specific responsibility in actively explaining the background and the benefits of their products.
Implementer: Member States, Industry, Academia, Civil society, EFSA, EMEA, Commission
Timeframe: 2002 onwards
Developing life sciences and biotechnology in harmony with ethical values and societal goals
Action 14
The Commission will strengthen and focus Community support for research into socio-economic and ethical issues and dissemination of results, including criteria for assessing the benefits of using biotechnology in agri-food production, to facilitate future reporting and to provide a good basis for societal decisions on the application of biotechnology and life sciences. The Commission will program research support to a more systematic mapping of benefits and disadvantages/risks which should include a strong component for dissemination of information and debate.
The Commission will ensure that ethical, legal and social implications are taken into account at the earliest possible stages of Community supported research by means of funding bioethics research and of providing an ethical review of research proposals received.
Implementer: Commission
Timeframe: 2002-2006
Action 15
The Commission proposes to enhance the role of the European Group on Ethics. In addition, the Commission will launch a separate consultation of the other Community institutions on possible structural and procedural improvements. The Commission will also promote collaboration between Community, national and local levels by promoting networking of national and local ethical bodies and elected representatives. The Commission will organise a network of academic and professional experts for ad-hoc advice on specific socio-economic aspects.
Implementer: Ethical bodies, Legislatures, Commission
Timeframe: 2002
Action 16
The Commission will develop, jointly with the EP, outreach measures to inform about the analysis of ethical issues at the EU level.
While respecting cultural pluralism, the Commission will work with public and private partners to identify areas where it is possible to establish consensus on ethical guidelines/standards or best practise. Areas might include stem cell research, biobanks, xenotransplantation, genetic testing and use of animals in research. Such guidelines could, when appropriate, take the form of self-regulatory initiatives in the scientific community and industry.
Implementer: European Parliament, Member States, Regions, Industry, Institutions, Commission
Timeframe: 2002 onwards
Demand-driven applications through informed choice
Action 17
The Commission will take initiative to develop, in partnership with Member States, farmers and other private operators, research and pilot projects to clarify the need, and possible options, for agronomic and other measures to ensure the viability of conventional and organic farming and their sustainable co-existence with genetically modified crops. Moreover, the Commission recognises the importance of safeguarding the existing genetic resources in agriculture. It will launch a new action programme for the conservation, characterisation, collection and utilisation of genetic resources in agriculture in the Community.
Implementer: Member States, professional associations, other operators, Commission
Timeframe: 2002 onwards
Confidence in science-based regulatory oversight
Pharmaceutical legislation
Action 18
Parliament and Council are invited to speed up the adoption of the three legislative proposals, revising the Community pharmaceutical legislation, including measures:
a) to develop and reinforce the system of giving scientific advice and to increase the access of the European Agency for Evaluation of Medicinal Products' (EMEA) scientific committees to high level expertise through the creation of expert panels and permanent working groups. The increased level of expertise will also help the revision and development of European guidelines on the quality, safety and efficacy aspects of biotechnological medicinal products.
b) to introduce an accelerated procedure for products with a major public health interest that will allow the assessment and authorisation of a medicinal product within a shortened time scale
c) to introduce a procedure allowing a conditional authorisation valid for one year, but renewable. This will allow products of major public health interest but for which certain studies are still in progress to be given a conditional access to the market during the finalisation of the studies.
Implementer: European Parliament, Council Timeframe: 2002
Genetically modified organisms (GMO) legislation
Short-term regulatory actions
Action 19
Parliament and Council are invited to speed up the adoption of the two following legislative proposals:
a) Proposal for a European Parliament and Council Regulation on Traceability and Labelling of Genetically Modified Organisms and Traceability of Food and Feed derives from Genetically Modified Organisms.
b) Proposal for a European Parliament and Council Regulation on Genetically Modified Food and Feed.
Implementer: European Parliament, Council
Timeframe: 2002
Action 20
The Commission continues its work with a view to finalising the legislative proposals which have already been announced, such as initiatives concerning GM plant propagating material, environmental liability and the implementation of the biosafety protocol.
Implementer: European Parliament, Council, Commission
Timeframe: 2002-2003
Implementation and enforcement activities
Action 21
The Commission will ensure that legislation is enforced in a uniform and effective way across the Community and adopt appropriate implementing measures required under relevant legislation, including the necessary guidance for detection and sampling methodology. The Commission will also establish a molecular register that is accessible to the public, containing information on events of genetic modification.
Implementer: Commission
Timeframe: 2002-2003
Specific long term regulatory actions
Action 22
The Commission will report on the feasibility of options to improve further the consistency and efficiency of the framework for authorising GMO's for deliberate release into the environment, including a centralised Community authorisation procedure.
Implementer: Commission
Timeframe: 2003
Action 23
The Commission will support the development of methodologies for monitoring potential long-term environmental impacts of GMO's as compared with conventional crops, and methodologies for the monitoring of effects of genetically modified food and feed as compared with conventional food and feed. With the establishment of the European Food Safety Authority, the work on the early identification of emerging risks will be reinforced and upgraded.
Implementer: Commission
Timeframe: 2002 onwards
3. Europe in the world - responding to global challenges
A European agenda for international collaboration
Action 24
The Commission should continue to play a leading role in developing international guidelines, standards and recommendations in relevant sectors, based on international scientific consensus and, in particular, push for the development of a consistent, science-based, focused, transparent, inclusive and integrated international system dealing with food safety issues.
Implementer: Commission
Timeframe: 2002 onwards
Europe's responsibilities towards the developing world
Agriculture
Action 25
The Commission will in co-operation with Member States support:
a) the redefining of national research towards an appropriate mix of traditional techniques and new technologies, based on priorities developed with local farmers.
b) the establishment of effective research partnerships between public and private research organisations in developing countries and in the EU, and the adequate capacity and infrastructure for developing countries to enter into such partnerships, in accordance with international commitments under the Conventions.
c) sub-regional, regional and international organisations, in particular the International Agricultural Research Centres.
Implementer: Member States, Commission
Timeframe: 2002 onwards
Genetic resources
Action 26
The Commission and the Member States will support the conservation and sustainable use of genetic resources in developing countries and their equitable sharing of benefits arising from their use by:
a) supporting the development and enforcement of effective measures to conserve, to use sustainably and to provide access to genetic resources and traditional knowledge, as well as to share equitably the benefit arising from them, including income generated by intellectual property protection. Support for local communities is vital to conserve indigenous knowledge and genetic resources.
b) supporting the participation of delegates from developing countries in the negotiations of relevant International Conventions.
c) supporting measures to promote greater regional co-ordination in legislation to minimise disparities in access, benefits and also trade in products derived from genetic resources, in accordance with international commitments.
Implementer: Member States, Commission
Timeframe: 2002 onwards
Health
Action 27
The Commission and the Member States should work with the international community to concretise the commitment to research to combat HIV/AIDS, Malaria, TB and other main poverty-related diseases and also identify effective measures to support developing countries in establishing the structures needed to deploy a health policy.
Implementer: Member States, Commission Timeframe: 2002 onwards
Responsible and careful use
Action 28
The Commission should support:
a) the safe and effective use of modern biotechnologies in developing countries, based on their autonomous choice and on their national development strategies.
b) measures to increase the capacity of developing countries to assess and manage risk for man and the environment, under conditions prevailing in the country.
c) the development of appropriate administrative, legislative and regulatory measures in the developing countries, for the proper implementation of the Cartagena Protocol.
d) that international research on social, economical and environmental impacts are effectively adapted to take into account conditions prevailing in developing countries and that the findings are subsequently disseminated to them in an appropriate format.
e) that the international regulatory requirements remain manageable by developing countries, so as not to impede their trade and production prospects.
Implementer: Commission
Timeframe: 2002 onwards
4. Implementation and coherence across policies, sectors and actors
Action 29
The Commission will enhance
a) the general foresight function across Commission services, and in particular its role in technology foresight through its Institute for Prospective Technological Studies (IPTS), for early identification of newly emerging issues and of elements of a policy response
b) its monitoring and review function to assess
- the relevance, coherence and effectiveness of legislation and policy
- the extent to which policy objectives are achieved and legislation enforced
- the societal and economic impact of legislation and policy measures.
In pursuit of these objectives and to further strengthen policy coherence, the Commission
c) will reinforce continuous co-ordination between its services and calls upon Member States to also provide enhanced foresight/review functions and a co-ordinated interface for a dialogue on these issues.
Implementer: Commission, Member States
Timeframe: From 2002 onwards
Action 30
The Commission will present a regular Report on Life Sciences and Biotechnology to monitor progress and indicate possible specific proposals to ensure policy and legislative coherence. The report will draw on the conclusions under actions 11 and 30.
Implementer: Commission
Timeframe: 2003 onwards