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Drug Master File
Results: 255

#	Item
111	ACCOUNTABILITY REPORT MASTER FILE Add to Reading List Source URL: scstatehouse.gov Language: English - Date: 2009-09-18 14:44:24 Center for Substance Abuse Treatment Drug rehabilitation Health Medicaid United States Department of Health and Human Services Government Substance abuse Health policy Substance Abuse and Mental Health Services Administration
112	DOC Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:21 Clinical research Research Science Food and Drug Administration Drug Master File Pharmaceutical formulation Clinical trial Abbreviated New Drug Application Excipient Pharmacology Pharmaceutical industry Pharmaceutical sciences
113	Quality Overall Summary - Chemical Entities (New Drug Submissions/Abbreviated New Drug Submissions) (QOS-CE (NDS/ANDS)) Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:26:08 Pharmaceutics Pharmacokinetics Clinical research Pharmaceuticals policy Bioequivalence Abbreviated New Drug Application Drug Master File Dosage form Good manufacturing practice Pharmacology Pharmaceutical sciences Pharmaceutical industry
114	DOC Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:21 Pharmaceutics Clinical research Pharmacokinetics Pharmaceuticals policy Drug Master File Excipient Dosage form Validation Bioequivalence Pharmaceutical industry Pharmaceutical sciences Pharmacology
115	Microsoft Word - draft_ebauche_dmf_fmm_guide_ld-eng.doc Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-12 14:25:40 Medicine Pharmaceutics Clinical research Drug Master File Pharmacology Natural Health Products Clinical trial Health Products and Food Branch Guidance document Pharmaceutical industry Health Canada Health
116	Untitled Document This content was archived on June 24, 2013. Archived Content Information identified as archived on the Web is for reference, research or recordkeeping purposes. It Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:26:08 Health Clinical research Research Medicinal chemistry Food and Drug Administration Drug Master File Pharmaceutical formulation Abbreviated New Drug Application Clinical trial Pharmaceutical sciences Pharmacology Pharmaceutical industry
117	Quality Overall Summary - Chemical Entities (Applications for Drug Identification Number Submission) (QOS-CE (DINA)) Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:26:08 Pharmacology Medicine Pharmaceuticals policy Validity Drug Master File Validation Excipient Dosage form Bioequivalence Pharmaceutical industry Pharmaceutical sciences Clinical research
118	Ministry Use Only Master File #: SUBMISSION SUMMARY Drug Products (Brand name/generic name/strengths): Add to Reading List Source URL: www.health.gov.on.ca Language: English - Date: 2013-05-22 14:04:45
119	DOC Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:21 Pharmacology Research Pharmaceuticals policy Validity Validation Excipient Drug Master File Dosage form Bioequivalence Pharmaceutical industry Pharmaceutical sciences Clinical research
120	USP Pending Monographs USP Pending Monographs Guideline, Version 2.7 Effective November 1, 2011 USP Pending Monographs: Objective Add to Reading List Source URL: www.usp.org Language: English - Date: 2012-08-29 09:41:13 Drugs Drug safety Medicine Academic publishing Monograph Drug reference standard Drug Master File New Drug Application USP Pharmacology Pharmaceutical sciences Pharmaceutical industry

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