This list is derived from a set of RAPS Regulatory Affairs Acronyms & Definitions publications for US, EU, Canada and international professionals. It includes more than 5,000 definitions from a variety of sources, specifying the region for each, cross-referenced for easy use. Entries were selected based on their relevance to professionals involved in all lifecycle stages for biologics, medicinal products, medical devices and related healthcare products.
 
This page is a valuable reference tool for those new to regulatory as well as experienced professionals. It is also a handy guide for those preparing for any of the RAC exams.
 
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