Medical Product Regulatory Affairs

Pharmaceuticals, Diagnostics, Medical Devices

Auteurs

• John J. Tobin

Paramètres

• 350 pages
• 13 heures de lecture

• Biologie
• Droit, Littérature juridique
• Littérature juridique
• Sciences naturelles

En savoir plus sur le livre

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

• Année de publication: 2023