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Australia Australia Therapeutics Goods Administration Brazil Ministerio da Saude Canada Health Canada Canadian Health Network Canadian Standardization Organization(CSA) Czech Republic Ministry of Health Czech Republic
European Union Eurolex; Database for Europan Law Europa; links to other EU and national government servers European Directives European Union GCP Directive European Union CEN Directive 95/46/EC EC Guidance Documents (MEDDEV) NB-MED Official Journal of the European Communities
Finland Finnish
France Agence pour la Diffusion de L'information Technologique
Germany Bundesinstitut für Arzneimittel und Medizinprodukte DIMDE Registered Ethics Committees
Hungary Hungary Ministry of health
Italy Ministerio della Sanita Dispositivi Medici
Sweden Medical Products Agency Guidance for Clinical Investigation of Medical Devices in Sweden
UK British Standardization Institute(BSI) Department of Health Medicines Control Agency(MHRA) Guidance : Information for Clinical Investigators
Japan Ministry of Health Ministry of Health, Labor and Welfare(MHLW) Notifications
Mexico Secretaria de Salud New Zealand Ministry of Health Switzerland The Federal Authorities of the Swiss Confederation United States AAHRPP ACHRE Report Bioresearch Monitoring FDA Center for Devices homepage GPO Gate, Federal Register Health & Human Services IHS Health Information Industry Portal to FDA Investigators Investigators Black List JCAHO--Joint Commission on Accreditation of Healthcare Organizations Code of Federal Regulations Development of Human Subject Research Policy Import/Export of Medical Devices National Bioethics Advisory Commission NIH Newsletter Office for Human Research Protection OHRP The Jungle Warning Letters 21 CFR part 860 Medical Device Classification procedure 21 CFR part 11.com Other International Standardization Organization(ISO) CIOMS GHTF Government Links Governments on the WWW
Information Resources
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Review Committees
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Societies and Publications
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Technology and Assessment Links
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This page was last updated on 03/27/08