Career Details
Description
The RAC (GS) exam is intended for regulatory professionals with 3-5 years of experience and is largely based upon knowledge and application of regulatory functions throughout the healthcare product lifecycle. It covers all product areas, including medical devices, IVDs, pharmaceuticals, medicinal products and biologics. Also covered on the exam are international standards and guidelines including those of ICH, GHTF, WHO and ISO.
Details
Certificates
Certificate name
Responsible Care AuditorCertifying Organization
Board of Environmental Health and Safety Auditor Certification
Type
B - Advanced
Certificate name
Certified IRB ProfessionalCertifying Organization
Public Responsibility in Medicine and Research
Type
B - Advanced
Certificate name
Certified FISMA Compliance PractitionerCertifying Organization
Federal Information Security Management Act Center
Type
A - Core
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