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Drug Master File
Results: 255

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201	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Impurity Materials Clinical research Drug Master File Pharmacology Food and Drug Administration Pharmaceutical sciences Pharmaceutical industry Environmental chemistry
202	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Clinical research Food and Drug Administration Pharmaceuticals policy Abbreviated New Drug Application Generic drug New Drug Application Drug Master File Pharmaceutical sciences Pharmaceutical industry Pharmacology
203	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Medicine Pharmaceutical industry Health Pharmacology Drug safety Drug Master File New Drug Application Prescription Drug User Fee Act Federal Food Drug and Cosmetic Act Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy
204	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Pharmacology Health Drug safety Investigational New Drug New Drug Application Drug development Drug Master File Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
205	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Clinical research Medicine Pharmaceutics Pharmaceuticals policy Abbreviated New Drug Application New Drug Application Drug Master File Title 21 CFR Part 11 Generic drug Pharmaceutical industry Food and Drug Administration Pharmaceutical sciences
206	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Food and Drug Administration Pharmaceuticals policy New Drug Application Validation Over-the-counter drug Drug Master File Pharmaceutical industry Pharmaceutical sciences Clinical research
207	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Research Clinical research Pharmaceuticals policy Drug safety Abbreviated New Drug Application Drug Master File Generic drug New Drug Application Food and Drug Administration Pharmaceutical industry Pharmaceutical sciences
208	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Abbreviated New Drug Application Dissolution testing Generic drug Food and Drug Administration Drug Master File New Drug Application Bioequivalence Bioavailability Pharmaceutical sciences Pharmaceutical industry Pharmacology
209	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Medicine Food and Drug Administration Dosage forms Clinical research Excipient Pre-clinical development Center for Biologics Evaluation and Research Center for Drug Evaluation and Research Drug Master File Pharmaceutical sciences Pharmacology Pharmaceutical industry
210	Common Technical Document – Quality Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:15 Pharmacology Pharmaceutical sciences Validation Drug Master File Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use HTML element Substance abuse Clinical trial Clinical research Pharmaceutical industry Research

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