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RAPS RAC-US Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Quality Systems and Regulatory Operations | - GxP systems (GMP, GCP, GLP) - Inspections and regulatory audits |
| Postmarket Compliance | - Pharmacovigilance and adverse event reporting - Device vigilance and recalls |
| Product Development Lifecycle | - Clinical trial frameworks and submissions (IND/IDE) - Drug and device development stages |
| Regulatory Foundations | - US regulatory structure and agencies (FDA overview) - Regulatory ethics and compliance principles |
| Premarket Requirements | - Marketing authorization pathways (NDA, ANDA, PMA, 510(k)) - Labeling and promotional compliance |
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