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History. In the 1980s the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.
The IEEE International Electron Devices Meeting (IEDM) is an annual micro- and nanoelectronics conference held each December that serves as a forum for reporting technological breakthroughs in the areas of semiconductor and related device technologies, design, manufacturing, physics, modeling and circuit-device interaction. [1]
The Global Harmonization Task Force ( GHTF) was “a voluntary group of representatives from national medical device regulatory authorities (such as the U.S. Food and Drug Administration (FDA)) and the members of the medical device industry ” [1] whose goal was the standardization of medical device regulation across the world.
The IEEE MTT-S International Microwave Symposium (IMS) is an annual technical professional conference specializing in RF / Microwave theory and applications that is a combination of multiple technical conferences and a commercial exhibition. The IMS is the largest gathering of RF/Microwave professionals in the world (7,300 to 12,000 total ...
The Council for International Organizations of Medical Sciences ( CIOMS) is an international non-governmental organization of 40 international, national, and associate member groups representing the biomedical science community. [1] It was jointly established by the World Health Organization (WHO) and United Nations Educational, Scientific and ...
BRUSSELS (Reuters) -The European Commission launched a probe into China's public procurement of medical devices on Wednesday, the latest in a series of moves that ratchet up trade tensions ahead ...
The third edition of ISO 14971 was published in December 2019 and supersedes the second edition of ISO 14971. [6] Specifically, ISO 14971 is a nine-part standard which first establishes a framework for risk analysis, evaluation, control, and review, and also specifies a procedure for review and monitoring during production and post-production.
The major International Conference of the Federation is now titled the World Congress. Meetings of the Federation are combined with those of the Organization for medical Physics (IOMP) and co-ordinated by the Conference Co-ordinating Committee of the International Union for Physics and Engineering Sciences in Medicine (IUPESM).
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