Whether you are new to EU Regulatory Affairs, preparing for the RAC (EU) Exam or looking for an update on the regulatory requirements in your field, the Fundamentals of EU Regulatory Affairs, Fourth Edition is an excellent reference tool that can put you on the right career path. This essential text provides a comprehensive understanding of established regulatory requirements across product lines for the EU.

New in 2008, this fourth edition has been expanded to help you continue in your path to reach your potential as a regulatory professional with:  

• New chapters  on medical device clinical trials, medicinal product clinical trials and the Paediatric Regulation
• Expanded chapters on authorization procedures for medical devices and medicinal products
• Updated facts, regulations and statistics
• Glossary of terms
• Contributions from volunteers well-renowned in the profession

SAVE! Purchase Fundamentals of EU Regulatory Affairs, Fourth Edition as a part of the following packages and save up to 20%:

• EU RAC Reference Package: Basic
• EU RAC Reference Package: Device Focus
• EU RAC Reference Package: Pharmaceutical Focus
• EU RAC Reference Package: Device and Pharmaceuticals

Copyright 2008, RAPS

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