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181	Baxter Healthcare Comments to the Proposed Safety Reporting Requirements for Human Drug and Biological Products: Proposed Rules October 14, 2003 Section FR Page Number Comment[removed]c)(2)(v)(C) (vi) & (vii) 12474 The r Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:40 Clinical research Research Pharmaceutical industry Clinical pharmacology United States Public Health Service MedDRA MedWatch Adverse event Adverse Event Reporting System Pharmacology Pharmaceutical sciences Food and Drug Administration
182	Comments from the MedDRA Maintenance and Support Services Organization on the Proposed Rule: Safety Reporting Requirements for Human Drug and Biologic Products (the “Tome”) Federal Register Vol. 68, No. 58, 14 Marc Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-11-04 17:23:27 Health Clinical research Pharmaceutical industry Drug safety Pharmacy MedDRA COSTART EudraVigilance IFPMA Pharmacology Pharmaceutical sciences Research
183	Ref: MedDRA 62 Annex 4 MSSO Written Comments to the FDA’s Proposed SADR Rule The MedDRA Maintenance and Support Services Organization (MSSO) supports the FDA’s proposal to use MedDRA® (Medical Dictionary for Regula Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-11-04 17:23:29 MedDRA Science GMDN Pharmacology Health Medicine
184	PRESS RELEASE Bids Invited for MedDRA Maintenance & Support Services Contract Geneva, August 15, 2014 – The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Hu Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-08-15 02:04:51 Pharmaceuticals policy Research Drug safety Pharmaceutical sciences International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Common Technical Document Pharmacology Clinical research MedDRA
185	Health Products and Food Branch Direction générale des produits de santé et des aliments Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:02:48 Clinical research Health in Canada MedDRA Food and Drug Administration Health Products and Food Branch Marketed health products directorate Health Canada Adverse Event Reporting System Pharmacology Pharmaceutical sciences Health
186	DOC Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:07 Medicine MedDRA COSTART WHOART Pharmacovigilance SNOMED CT Food and Drug Administration Systematized Nomenclature of Medicine Pharmaceutical industry Pharmacology Pharmaceutical sciences Health
187	SAFETY REQUIREMENTS FOR HUMAN DRUG AND BIOLOGICAL PRODUCTS General Comments Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:03:45 Health Food and Drug Administration Clinical research Drug safety MedDRA Pharmacovigilance MedWatch Package insert COSTART Pharmacology Pharmaceutical sciences Pharmaceutical industry
188	DOC Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-10-28 17:02:57 Transfusion medicine Patient safety Food and Drug Administration Hematology MedDRA Adverse Event Reporting System Blood transfusion Blood donation MSM blood donor controversy Medicine Health Pharmacology
189	Information Request PVP, December 18, [removed]Ruconest Add to Reading List Source URL: www.fda.gov Language: English Angiology Thrombosis Deep vein thrombosis Thrombus Embolism Pulmonary embolism Arterial embolism Stroke MedDRA Medicine Hematology Circulatory system
190	Understanding MedDRA The Medical Dictionary for Regulatory Activities What is ICH? The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (www.ich Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-09-17 11:47:48 Research Clinical research Drug safety Pharmaceutical industry Pharmaceuticals policy MedDRA EudraVigilance IFPMA Pharmacovigilance Pharmacology Pharmaceutical sciences Health