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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.
Canadian Regulatory Acronyms & Definitions, Fifth Edition, gives professionals working in the Canadian market a competitive advantage across the regulatory arena. Compiled by RAPS, it is filled with entries of significance to the Canadian healthcare product industry. Regulatory professionals involved in all lifecycle stages of biologics, medicinal products, medical devices and more will find exactly what they’re looking for in the pages of this handy reference guide.
Who Should Use This Publication?
This reference is a valuable resource for regulatory professionals who are new to the Canadian market and seasoned pros.
Published by RAPS © 2016. Paperback. 96 pages.