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Medical Products Agency
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#	Item
111	On the use of Amalgam for dental fillings in Sweden Lennart Philipson, Ph.D. Director Medical Devices Medical Products Agency Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-09-18 15:33:01 Medical technology Mercury Lennart Medical device Notified Body Philipson Amalgam Medicine Technology Medical equipment
112	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. It was current when produced, but is no longer maintained and may Add to Reading List Source URL: www.fda.gov Language: English Clinical research Department of Health Medicines and Healthcare products Regulatory Agency Pharmaceutical industry Commission on Human Medicines Food and Drug Administration Medical device Yellow Card Scheme Pharmaceutical sciences Medicine Pharmacology
113	Memorandum D19-9-1 Ottawa, August 20, 2014 Importation of Human Drugs, Natural Health Products, and Medical Devices Regulated by the Food and Drugs Act Add to Reading List Source URL: cbsa.gc.ca Language: English - Date: 2014-08-25 10:12:49 Pharmacology Pharmaceuticals policy Food law Pharmacy Clinical pharmacology Food and Drugs Act Canada Border Services Agency Natural health product Regulation of therapeutic goods Medicine Health Pharmaceutical sciences
114	Submitted via www.regulations.gov August 25, 2014 Attn: Bakul Patel Division of Dockets Management (HFA-305) Food and Drug Administration 5630 Fishers Lane, rm. 1061 Add to Reading List Source URL: www.tiaonline.org Language: English - Date: 2014-08-25 15:26:25 Medical equipment Medical device Food and Drug Administration Quality management system Patient safety GMDN Medicines and Healthcare products Regulatory Agency Medicine Health Medical technology
115	To: European Medicines Agency, EMA Copy: European Commission (DG SANCO) Copy: Medicines and Healthcare products Regulatory Agency – MHRA, UK Copy: Other Medical Agencies in Europe Copy: Media Add to Reading List Source URL: jannel.se Language: English - Date: 2010-11-07 11:58:04 Chemistry Amines Clinical research Pharmaceutical industry Atomoxetine Nootropics Medicines and Healthcare products Regulatory Agency European Medicines Agency Food and Drug Administration Pharmaceutical sciences Pharmacology Eli Lilly and Company
116	Memorandum D19-9-1 Ottawa, August 20, 2014 Importation of Human Drugs, Natural Health Products, and Medical Devices Regulated by the Food and Drugs Act Add to Reading List Source URL: cbsa-asfc.gc.ca Language: English - Date: 2014-08-25 10:12:49 Pharmacology Pharmaceuticals policy Food law Pharmacy Clinical pharmacology Food and Drugs Act Canada Border Services Agency Natural health product Regulation of therapeutic goods Medicine Health Pharmaceutical sciences
117	Report of the workshop on the regulation of regenerative medicine Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-05-24 11:21:05 Stem cells Clinical research Emerging technologies Cell therapy European Medicines Agency Medicines and Healthcare products Regulatory Agency Regenerative medicine Medical Research Council Stem cell Biology Biotechnology Pharmaceutical industry
118	Memorandum D19-9-1 Ottawa, August 20, 2014 Importation of Human Drugs, Natural Health Products, and Medical Devices Regulated by the Food and Drugs Act Add to Reading List Source URL: www.asfc-cbsa.gc.ca Language: English - Date: 2014-08-25 10:12:49 Pharmacology Pharmaceuticals policy Food law Pharmacy Clinical pharmacology Food and Drugs Act Canada Border Services Agency Natural health product Regulation of therapeutic goods Medicine Health Pharmaceutical sciences
119	Memorandum D19-9-1 Ottawa, August 20, 2014 Importation of Human Drugs, Natural Health Products, and Medical Devices Regulated by the Food and Drugs Act Add to Reading List Source URL: asfc.gc.ca Language: English - Date: 2014-08-25 10:12:49 Pharmacology Pharmaceuticals policy Food law Pharmacy Clinical pharmacology Food and Drugs Act Canada Border Services Agency Natural health product Regulation of therapeutic goods Medicine Health Pharmaceutical sciences
120	ANNEX PROPOSAL FOR A DIRECTIVE AMENDING, AS REGARDS INFORMATION TO THE GENERAL PUBLIC ON MEDICINAL PRODUCTS SUBJECT TO MEDICAL PRESCRIPTION, DIRECTIVE[removed]EC The draft proposal focuses on information as to the: Add to Reading List Source URL: haieurope.org Language: English - Date: 2010-12-02 11:09:36 Health Medicine Clinical research Summary of Product Characteristics Medical prescription Directive 2001/83/EC Prescription medication European Medicines Agency Supplementary protection certificate Pharmaceuticals policy Pharmaceutical sciences Pharmacology

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