Drug Master File

Results: 255



#Item
61Professional certification / Master of Education / Licensed professional counselor / Science / Licensure / Occupations / Sociology

PROPOSED REGULATION OF THE BOARD OF EXAMINERS FOR ALCOHOL, DRUG AND GAMBLING COUNSELORS LCB File No. R058-14 July 31, 2014 EXPLANATION – Matter in italics is new; matter in brackets [omitted material] is material to be

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Source URL: www.leg.state.nv.us

Language: English - Date: 2014-08-01 14:08:55
62Professional certification / Master of Education / Licensed professional counselor / Science / Licensure / Occupations / Sociology

PROPOSED REGULATION OF THE BOARD OF EXAMINERS FOR ALCOHOL, DRUG AND GAMBLING COUNSELORS LCB File No. R058-14 July 31, 2014 EXPLANATION – Matter in italics is new; matter in brackets [omitted material] is material to be

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Source URL: www.leg.state.nv.us

Language: English - Date: 2014-08-01 14:08:55
63Professional certification / Master of Education / Licensed professional counselor / Science / Licensure / Occupations / Sociology

PROPOSED REGULATION OF THE BOARD OF EXAMINERS FOR ALCOHOL, DRUG AND GAMBLING COUNSELORS LCB File No. R058-14 July 31, 2014 EXPLANATION – Matter in italics is new; matter in brackets [omitted material] is material to be

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Source URL: leg.state.nv.us

Language: English - Date: 2014-08-01 14:08:55
64Pharmacology / Health / Clinical research / Drug safety / Supplementary protection certificate / European Medicines Agency / Qualified Person for Pharmacovigilance / Drug Master File / Marketing authorization / Pharmaceutical sciences / Pharmaceuticals policy / Pharmaceutical industry

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL

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Source URL: www.lakemedelsverket.se

Language: English - Date: 2009-03-19 06:42:41
65Medicine / 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

Guidance for Industry and Reviewers Repeal of Section 507 of the Federal Food, Drug, and Cosmetic Act U.S. Department of Health and Human Services

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Source URL: www.fda.gov

Language: English
66Pharmaceuticals policy / Pharmacology / Pharmaceutics / Therapeutics / Prescription Drug User Fee Act / Center for Drug Evaluation and Research / Drug Master File / Generic drug / Abbreviated New Drug Application / Food and Drug Administration / Pharmaceutical industry / Pharmaceutical sciences

GDUFA Public Mtg Min[removed]

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Source URL: www.fda.gov

Language: English
67Pharmacology / Pharmaceutics / Pharmaceuticals policy / Therapeutics / New Drug Application / Drug Master File / Generic drug / Prescription Drug User Fee Act / Form FDA 483 / Pharmaceutical industry / Pharmaceutical sciences / Food and Drug Administration

December 20, 2010: FDA Update regarding Generic Drug User Fees

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Source URL: www.fda.gov

Language: English
68Medicine / Pharmaceuticals policy / Health / Abbreviated New Drug Application / Drug safety / Drug Master File / Drug Price Competition and Patent Term Restoration Act / New Drug Application / Anda / Pharmaceutical industry / Pharmaceutical sciences / Food and Drug Administration

Pre-ANDA Litigation, Chapter 18: ANDA Preparation (with an Eye toward Approval and Litigation) and the FDA Review

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Source URL: www.duanemorris.com

Language: English - Date: 2014-08-11 11:16:58
69Pharmaceutical sciences / Health / Medicine / Food law / United States Public Health Service / Drug Master File / Federal Food /  Drug /  and Cosmetic Act / Abbreviated New Drug Application / Fee / Food and Drug Administration / Pharmaceuticals policy / Pharmaceutical industry

tkelley on DSK3SPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Friday, August 1, [removed]Notices The application or supplement fee for a biosimilar biological product is due upon submission of the applicati

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Source URL: www.gpo.gov

Language: English - Date: 2014-10-06 16:33:48
70Medicine / Pharmacology / Pharmaceutical industry / Drug safety / Pharmaceuticals policy / Investigational New Drug / Quality by Design / Treatment IND / Drug Master File / Food and Drug Administration / Health / Pharmaceutical sciences

CDER Regulatory Applications – Investigational New Drug and New Drug Applications

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Source URL: www.fda.gov

Language: English
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