|
Created in 1968 as a non-profit, non-governmental organisation
(NGO), the International Federation of Pharmaceutical Manufacturers
(IFPMA) represents, through its member associations and companies, the international
worldwide research-based pharmaceutical industry and manufacturers
of prescribed medicines.
Member Associations
The members of IFPMA are national or regional pharmaceutical industry
associations in over 60 countries of both the industrialised and
developing world. The conditions for membership of the Federation
include commitments by the association, on behalf of its members,
to good manufacturing practices and acceptance of the provisions
of the IFPMA Code of Pharmaceutical Marketing Practices.
Member Companies
As of November 2004, pharmaceutical companies can become members of IFPMA. The conditions for a pharmaceutical company's membership of the Federation include:
- its undertaking substantial research and development of innovative medicines and vaccines in relation to total activities;
- its adoption of and adherence to the IFPMA Marketing Code;
- its support of adequate and effective intellectual property protection and science-based regulatory practices worldwide;
- its membership in the IFPMA association in the country of its Headquarters, where such an association exists.
The pharmaceutical industry, represented by IFPMA, is committed
to the research and development and quality manufacturing of innovative
therapeutic medicines that save lives, reduce overall health care
costs and improve the quality of life of people around the world.
The industry strives to create a global environment that fosters:
innovation in preventing and curing diseases; drug regulation that
expedites approvals of new chemical and biological treatments for
patients and assures the availability of genuine quality medicines;
patient access to innovative therapies and protection from substandard
and counterfeit products; market-based competition in the health
care sector; and, the dissemination of drug information and ethical
promotion of drugs to medical professionals and, where legal, to
patients.
The IFPMA membership believes that a viable, research-based pharmaceutical
industry operating in an open market -- with adequate and effective
protection of intellectual property in line with other industries
and with regulatory policies designed to ensure the rapid introduction
of new chemical and biological products -- is essential to patients'
well-being and to economic development of all countries around the
world.
The IFPMA carries out its mission through:
- fact-gathering and analysis of the policy issues of major importance
to industry;
- advocating policies supporting intellectual property protection,
market competition, drug regulation and access to information
about new therapies;
- encouraging measures consistent with the objectives of industry
and patients stated above;
- co-ordinating and leading member association and industry efforts
to achieve an environment conducive to therapeutic innovation
and competition;
- providing timely information to its members; and,
- diligently overseeing the implementation of the IFPMA Code of
Pharmaceutical Marketing Practices.
IFPMA is a non-for-profit and non-governmental organisation that
gives much emphasis to co-operation with UN agencies and other international
organisations concerned with health and trade-related issues.
IFPMA has achieved consultative status with the United Nations
and international organisations such as: the World Health Organisation,
(WHO), the World Intellectual Property Organisation (WIPO), the
World Trade Organisation (WTO) the United Nations Conference on
Trade and Development (UNCTAD), the United Nations Industrial Development
Organisation (UNIDO) the United Nations Economic and Social Council
(ECOSOC), the United Nations Children's Fund (UNICEF) and the Council
of Europe.
IFPMA has five working committees:
- Innovation, Intelectual Property and Trade Committee (IIPT)
- Partnerships, Public Health and Advocacy Committee (PPHA)
- Health Care Systems Committee (HCS)
- Regulatory Policy and Technical Standards Committee (RPTS)
- Biologicals and Vaccines Committee (B&V)
Ad
hoc groups are convened when required, to undertake specific tasks,
such as the preparation of publications and symposia.
|