Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 166,57
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In den WarenkorbZustand: New. In.
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In den WarenkorbGebunden. Zustand: New. Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. At a time when pharmaceutical companies are reviewing their R&D strategies, and attempting to reduce drug development times, it is .
Sprache: Englisch
Verlag: Kluwer Academic Publishers, 1996
ISBN 10: 0792387066 ISBN 13: 9780792387060
Anbieter: Kennys Bookstore, Olney, MD, USA
Zustand: New. Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. The proceedings of the 11th CMR Workshop, held in September 1995 and reproduced in this book, provide an overview of the current review process around the world. Editor(s): Lumley, C.E.; Walker, Stuart R. Series: Centre for Medicines Research Workshop. Num Pages: 172 pages, biography. BIC Classification: MMG; TDCW. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly. Dimension: 297 x 210 x 12. Weight in Grams: 454. . 1996. Hardback. . . . . Books ship from the US and Ireland.
Sprache: Englisch
Verlag: Springer Nature B.V. Apr 1996, 1996
ISBN 10: 0792387066 ISBN 13: 9780792387060
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - Regulatory review is the last major development hurdle that must be passed by a new medicine before it reaches the market. At a time when pharmaceutical companies are reviewing their R&D strategies, and attempting to reduce drug development times, it is extremely important that the review process is made as efficient as possible. The 11th CMR Workshop, held in September 1995, provided the opportunity for regulatory authority and industry personnel from Europe, North America, Australia and Japan to openly discuss views and exchange experiences on the subject of improving the review process. The proceedings of this meeting provide a comprehensive overview of the current review process around the world. The contributors describe the present situation and highlight company strategies and regulatory initiatives to improve the review process. This volume also summarises the suggestions that were developed by the participants, covering many facets of this process, including the quality and size of the dossier, dialogue, submission strategies, feedback and the response to questions.