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The Regulatory Affairs Certification (RAC) is the leading credential for regulatory professionals in the healthcare sector. The two RAC designations are Pharmaceuticals (RAC-Drugs) and Medical Devices (RAC-Devices). The RAC is intended for individuals employed in regulatory agencies, industry, consultancies and other settings involved with the regulation of healthcare products.
The Regulatory Compliance Certifications are credentials designed by regulatory professionals for regulatory professionals. There are two RCC exams: The RCC-IVDR and the RCC-MDR. This designation provides third-party validation, indicating that a certification holder understands European regulations for in vitro diagnostics (IVDs) or medical devices.
Show the world that you have the foundational knowledge regulatory affairs professionals need. The new Foundation in Regulatory Affairs (FRA) assessment-based certificate is designed to help you build regulatory affairs knowledge and then test that knowledge through an exam.
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