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Drug Master File
Results: 255

#	Item
181	Drug Master File (DMF) Application Form Drug Master File (DMF) Name: Add to Reading List Source URL: www.hc-sc.gc.ca - Date: 2013-12-13 09:48:37
182	Drug Master File (DMF) Application Form Add to Reading List Source URL: www.hc-sc.gc.ca - Date: 2013-06-24 11:49:32
183	Federal Register / Vol. 78, No[removed]Friday, August 2, [removed]Notices FDA is committed to the orderly conduct of its advisory committee meetings. Please visit our Web site at http://www.fda.gov/ AdvisoryCommittees/ Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-08-02 02:50:31 Pharmaceuticals policy Medicine Health Pharmacology Food law Drug Master File Federal Food Drug and Cosmetic Act Generic drug New Drug Application Pharmaceutical industry Pharmaceutical sciences Food and Drug Administration
184	pmangrum on DSK3VPTVN1PROD with[removed]Federal Register / Vol. 78, No[removed]Thursday, January 17, [removed]Notices Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-01-17 04:04:46 Health Pharmaceutical industry Food and Drug Administration Food law Therapeutics Drug Master File Generic drug Federal Food Drug and Cosmetic Act Abbreviated New Drug Application Pharmaceuticals policy Pharmaceutical sciences Medicine
185	Guidance for Industry Nonclinical Studies for the Safety Evaluation of Pharmaceutical Excipients U.S. Department of Health and Human Services Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-05-17 14:00:17 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
186	erowe on DSK2VPTVN1PROD with Federal Register / Vol. 77, No[removed]Thursday, October 25, [removed]Notices ANDA and PAS fees will make up 24 percent of the $249,000,000, which is $59,760,000. Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2012-10-25 00:48:06 Pharmaceuticals policy Medicine Health Food law Pharmacology Abbreviated New Drug Application Federal Food Drug and Cosmetic Act Drug Master File New Drug Application Pharmaceutical industry Pharmaceutical sciences Food and Drug Administration
187	User Fees Donal Parks, MBA, MPM Director User Fee Collections Staff Office of Management Add to Reading List Source URL: www.fda.gov Language: English Prescription Drug User Fee Act Fee Abbreviated New Drug Application Patent application User fee Credit card Anda Business Taxation in the United States Drug Master File Pharmaceutical industry
188	Therapeutic Products Directorate To: [Name], Director, Office of Clinical Trials Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:21 Clinical research Pharmaceutics Research Drug Master File Pharmaceutical formulation Excipient Dosage form Validation Good manufacturing practice Pharmaceutical industry Pharmaceutical sciences Pharmacology
189	Therapeutic Products Directorate To: [Name], Director, Office of Clinical Trials Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:20 Clinical research Pharmaceutics Pharmaceuticals policy Food and Drug Administration Drug Master File Pharmaceutical formulation Excipient Dosage form Validation Pharmaceutical industry Pharmaceutical sciences Pharmacology
190	Drug Master File (DMF) Application Form Add to Reading List Source URL: www.hc-sc.gc.ca - Date: 2013-12-13 10:07:56

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