Pharmaceutical Product Licensing (PDF)
Requirements for Europe
(Sprache: Englisch)
Provides a systematic account of the major technical, administrative and legal requirements for registering a product in any of the national markets within the EEC, using the existing procedures, with guidance as to how these procedures are likely to change after 1992.
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Provides a systematic account of the major technical, administrative and legal requirements for registering a product in any of the national markets within the EEC, using the existing procedures, with guidance as to how these procedures are likely to change after 1992.
Autoren-Porträt von A. C. Cartwright
Anthony C. Cartwright spent 14 years in pharmaceutical research and development before joining the British Pharmacopoeia Commission. He has worked in almost every area of product licensing and is currently Superintendent Pharmacist at the Medicines Control Agency, London. He is Chairman of the Quality Working Party of the Committee for Proprietary Medicinal Products (CPMP). Brian R. Matthews joined the British Pharmacopoeia Commission Secretariat in 1975 and the Product Licensing Pharmaceutical Secretariat in 1981. His interest in radiopharmaceutical products has led to his involvement in a European Commission Working Group on Radiopharmaceuticals, which advises the CPMP on requirements for these products: he moved to Alcon Laboratories from the Medicines Control Agency in 1992.
Bibliographische Angaben
- Autor: A. C. Cartwright
- 1991, 328 Seiten, Englisch
- Herausgegeben: Brian R. Matthews, Anthony C. Cartwright
- Verlag: Taylor & Francis
- ISBN-10: 0203984005
- ISBN-13: 9780203984000
- Erscheinungsdatum: 31.05.1991
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- Größe: 23 MB
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Englisch
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