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More Than 300 Earn Regulatory Affairs Certification (RAC), the Only Professional Certification for the Healthcare Product Regulatory Field
Date:1/14/2010

n">Sherry Keramidas, Ph.D., CAE. "The myriad roles regulatory professionals play are often invisible to the general public but their contributions are critically important to pharmaceuticals, medical devices and other healthcare products we use every day."

RAC-credentialed professionals are among the current and rising leaders in the regulatory profession. They work in all parts of the world and in many settings, including industry, government and academic organizations. As evidence that the credential's prominence and importance is increasing, registrations for the RAC exam are on the rise. Registration for the spring 2010 exam period is currently open and more information can be found online at RAPS.org/rac. The RAC exam is intended for regulatory professionals with three to five years of regulatory experience.

Four different RAC certifications are available: the RAC (US) covering U.S. regulations, the RAC (EU) covering European regulations, the RAC (CAN) covering Canadian regulations and the RAC (General Scope), which covers general regulatory responsibilities and international standards.

About RAPS

The Regulatory Affairs Professionals Society (RAPS) is an international membership organization of regulatory professionals in the rapidly growing medical device, pharmaceutical and biotechnology sectors. Regulatory professionals play vital roles in making better healthcare products possible. They work throughout the healthcare product lifecycle, ensuring these products are safe and effective, while driving organizational strategy and sound decision-making. RAPS supports these individuals and the regulatory profession by providing education a
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SOURCE Regulatory Affairs Professionals Society (RAPS)
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