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Drug Master File
Results: 255

#	Item
121	ACCOUNTABILITY REPORT MASTER FILE Add to Reading List Source URL: www.scstatehouse.gov Language: English - Date: 2013-09-24 11:34:09 Substance Abuse and Mental Health Services Administration United States Department of Health and Human Services Best practice Health care provider Center for Substance Abuse Treatment California Department of Alcohol and Drug Programs Health Medicine Substance abuse
122	Date: [removed]NOTICE Our file number: [removed]Health Canada is pleased to announce the release of the following draft documents for Stakeholder Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:25:38 Clinical research Research Pharmaceuticals policy Drug Master File Drug Identification Number Good manufacturing practice Common Technical Document Validation Regulatory requirement Pharmaceutical sciences Pharmaceutical industry Pharmacology
123	PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO-OPERATION SCHEME 17 November 2010 PRESS RELEASE PIC/S MEETINGS Add to Reading List Source URL: www.picscheme.org Language: English - Date: 2010-11-17 10:47:48 Pharmacology Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme Validation Medicines and Healthcare products Regulatory Agency Site Master File Good distribution practice Food and Drug Administration European Directorate for the Quality of Medicines Veterinary Medicines Directorate Pharmaceutical industry Pharmaceutical sciences Pharmaceutics
124	CGMP for PET Drugs - 21 CFR 212 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Title 21 of the Code of Federal Regulations Good manufacturing practice Center for Drug Evaluation and Research Positron emission tomography Investigational New Drug Validation Drug Master File Medicine Health Food and Drug Administration
125	Microsoft Word - int_drug_list_notice_avis_proc_int_exam-eng.docx Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:49:33 Screening Drug Master File Generic drug Drug discovery Electronic submission Pharmaceutical sciences Pharmaceutical industry Pharmacology
126	Microsoft Word - Variation Type IA and IB guideline rev.1 5 July[removed]doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2010-07-16 06:10:44 Validation Drug Master File Qualified Person Good manufacturing practice Health Science Business Pharmaceutical industry Clinical research Pharmaceuticals policy
127	DOC Document Add to Reading List Source URL: www.stoptb.org Language: English - Date: 2010-07-12 11:16:57 Pharmaceuticals policy Pharmacy Dosage forms Drug Master File Certificate of pharmaceutical product Good manufacturing practice Tablet Packaging and labeling Active ingredient Pharmaceutical sciences Pharmaceutical industry Pharmacology
128	PDF Document Add to Reading List Source URL: media.wiley.com Language: English - Date: 2013-08-31 10:13:40 Pharmacology Pharmaceuticals policy Clinical research Drug safety Regulatory requirement Validation Food and Drug Administration Bioequivalence Drug Master File Pharmaceutical industry Pharmaceutical sciences Health
129	DOC Document Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2011-04-15 10:50:58 Pharmaceuticals policy Clinical research Health Drug safety Qualified Person for Pharmacovigilance Drug Master File Qualified Person Medicinal product Pharmaceutical sciences Pharmacology Pharmaceutical industry
130	Microsoft Word - Addendum to the eCTD Backbone Files Specification for Module 1-v2 3 Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Drug safety Pharmaceutical industry Clinical Data Management Electronic Common Technical Document Investigational New Drug Drug Master File New Drug Application Food and Drug Administration Medicine Research

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