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This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Featuring entries selected by RAPS’ EU regulatory experts, EU Regulatory Acronyms & Definitions, Sixth Edition is a handy guide to the industry in the EU.
No matter your area of expertise—biologics, medicinal products, medical devices and more—RAPS helps regulatory professionals translate EU regulatory language into an invaluable reference guide.
Who Should Use This Publication?
Whether studying for the RAC (EU) or a longstanding member of the European regulatory field, this reference makes for a well-rounded professional library.
Published by RAPS © 2016. Paperback. 73 pages.