International Regulatory Acronyms & Definitions, Third Edition

Member: $10.00 Nonmember: $15.00
International Regulatory Acronyms & Definitions, Third Edition

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.

Add Book to Cart

Discover more of what matters to you

Advertising, Promotion and Labeling APIs Audit/FDA Inspection Biologics Biotechnology Chemistry, Manufacturing and Controls (CMC) Clinical Trials Combination Products Compliance Diagnostics Environmental Ethics FDA meeting and communication strategy Global Medical Devices Nutritional/Natural Health OTC Other Pharmaceuticals Preclinical study Product Lifecycle Project management Quality Assurance and Control Regulatory Intelligence/Policy Research, Design and Development Supply Chain Management

News »