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Drug Regulatory Affairs: Review
Introduction to regulatory affairs
Taschenbuch von Vinod Waghmare
Sprache: Englisch

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Beschreibung
Drug development to commercialization is highly regulated. Every drug before getting market approval must undergo rigorous scrutiny and clinical trials to ensure its safety, efficacy and quality. Regulatory department is crucial link between company, products and regulatory authorities. In today¿s competitive environment the reduction of the time taken to reach the market is vital to a product¿s and hence the company¿s success. The proper conduct of its Regulatory Affairs activities is therefore of considerable economic significance for the company. The success of regulatory strategy is less dependent on the regulations than on how they are interpreted, applied, and communicated within companies and to outside constituents. Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. In this book provides basic information regarding Regulatory Affairs- it¿s important in pharmaceutical industry, Responsibility of regulatory professions, list of various regulatory authorities and their regulations etc
Drug development to commercialization is highly regulated. Every drug before getting market approval must undergo rigorous scrutiny and clinical trials to ensure its safety, efficacy and quality. Regulatory department is crucial link between company, products and regulatory authorities. In today¿s competitive environment the reduction of the time taken to reach the market is vital to a product¿s and hence the company¿s success. The proper conduct of its Regulatory Affairs activities is therefore of considerable economic significance for the company. The success of regulatory strategy is less dependent on the regulations than on how they are interpreted, applied, and communicated within companies and to outside constituents. Regulatory Affairs plays a crucial role in the pharmaceutical industry and is involved in all stages of drug development and also after drug approval and marketing. In this book provides basic information regarding Regulatory Affairs- it¿s important in pharmaceutical industry, Responsibility of regulatory professions, list of various regulatory authorities and their regulations etc
Über den Autor
Mr. Vinod Vishnu Waghmare, M.Pharm (Pharmaceutics), from Shivaji University, Kolhapur. Currently he is working as Regulatory affairs -Manager in Galaxy Pharmaceuticals, Kenya.
Details
Erscheinungsjahr: 2019
Fachbereich: Toxikologie
Genre: Medizin
Rubrik: Wissenschaften
Medium: Taschenbuch
Seiten: 52
Inhalt: 52 S.
ISBN-13: 9786202057738
ISBN-10: 6202057734
Sprache: Englisch
Ausstattung / Beilage: Paperback
Einband: Kartoniert / Broschiert
Autor: Waghmare, Vinod
Hersteller: LAP LAMBERT Academic Publishing
Maße: 220 x 150 x 4 mm
Von/Mit: Vinod Waghmare
Erscheinungsdatum: 06.02.2019
Gewicht: 0,096 kg
preigu-id: 115848023
Über den Autor
Mr. Vinod Vishnu Waghmare, M.Pharm (Pharmaceutics), from Shivaji University, Kolhapur. Currently he is working as Regulatory affairs -Manager in Galaxy Pharmaceuticals, Kenya.
Details
Erscheinungsjahr: 2019
Fachbereich: Toxikologie
Genre: Medizin
Rubrik: Wissenschaften
Medium: Taschenbuch
Seiten: 52
Inhalt: 52 S.
ISBN-13: 9786202057738
ISBN-10: 6202057734
Sprache: Englisch
Ausstattung / Beilage: Paperback
Einband: Kartoniert / Broschiert
Autor: Waghmare, Vinod
Hersteller: LAP LAMBERT Academic Publishing
Maße: 220 x 150 x 4 mm
Von/Mit: Vinod Waghmare
Erscheinungsdatum: 06.02.2019
Gewicht: 0,096 kg
preigu-id: 115848023
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