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RAPS Offers New International Regulatory Affairs Certification - RAC (GS)
Date:4/7/2009

has become increasingly apparent."

RAC (GS) candidates must take an exam covering knowledge of the full product lifecycles for medical devices, IVDs, pharmaceutical and medicinal products, as well as international guidelines and standards such as those from ICH, GHTF, WHO and ISO. The first exam will be offered worldwide beginning in October.

For more information, visit www.raps.org/rac.

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. As regulatory professionals, RAPS members perform vital work in all areas of 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 as a whole by providing education and training, certification, professional standards, research, knowledge-sharing, publications, networking and career development opportunities and other valuable resources; and is committed to helping its members continually develop the knowledge and skills they need to excel. RAPS.org


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SOURCE Regulatory Affairs Professionals Society (RAPS)
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