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- 350pages
- 13 heures de lecture
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Building on the success of its predecessor, this second edition of the hands-on guide to how pharmaceutical and medical devices are regulated within the major global markets has an even wider scope and now features case studies. The new EU-framework and US regulations are also fully integrated. The textbook is based on a module prepared by the authors for an MSc course. This and its broad coverage make it an ideal resource for training purposes in both industry and academia. It is equally a valuable reference for all scientists needing to familiarize themselves with the topic.
Achat du livre
Medical Product Regulatory Affairs, John J. Tobin
- Langue
- Année de publication
- 2023
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- (rigide)
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- Titre
- Medical Product Regulatory Affairs
- Sous-titre
- Pharmaceuticals, Diagnostics, Medical Devices
- Langue
- Anglais
- Auteurs
- John J. Tobin
- Éditeur
- Wiley-VCH
- Publié
- 2023
- Format
- rigide
- Pages
- 350
- ISBN10
- 3527333266
- ISBN13
- 9783527333264
- Séries
- Mots clés
- Nonfiction, Sciences sociales, Commerce, Affaires & Gestion, Science et Mathématiques, Thématique juridique, Droit, Sciences naturelles, Biologie
- Description
- Building on the success of its predecessor, this second edition of the hands-on guide to how pharmaceutical and medical devices are regulated within the major global markets has an even wider scope and now features case studies. The new EU-framework and US regulations are also fully integrated. The textbook is based on a module prepared by the authors for an MSc course. This and its broad coverage make it an ideal resource for training purposes in both industry and academia. It is equally a valuable reference for all scientists needing to familiarize themselves with the topic.