Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at raps@raps.org if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
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.
Regulatory professionals speak a unique language that becomes even more complex in the international arena. RAPS’ handy guide to international regulatory terms, definitions and acronyms will help you develop a better understanding of the conversation.
International Regulatory Acronyms & Definitions, Third Edition, was developed by RAPS’ experts to include entries of primary interest to regulatory professionals involved in all aspects of international regulations. Whether you’re involved in the manufacture of drugs, biologics or medical devices, you’ll find comprehensive information and easy-to-use cross-references to help you become fluent in the diverse international regulatory arena.
Who Should Use This Publication?
Regulatory professionals who routinely pursue product lines beyond their domestic borders will find this reference resource an essential addition to their libraries.
Published by RAPS ©2016. Paperback. 40 pages.