Clinical Research Acronyms Quiz Test your knowledge of clinical research acronyms. Question Title * 1. ADR Adverse Drug Research Adverse Drug Reaction Adaptive Drug Relevance OK Question Title * 2. BSM Bioscience Management Biological Study Management Biospecimen Management OK Question Title * 3. CAPA Corrective and Preventive Action Clinical Award for Precision Analysis Complete, Accurate, Provable, Attributable OK Question Title * 4. CTRP Clinical and Translational Research Program Clinical Trial Regulatory Process Clinical Trials Reporting Program OK Question Title * 5. DSMB Data and Safety Monitoring Board Department of Safety and Medicine Board Department of Safety Monitoring Board OK Question Title * 6. EC Ethics Committee European Counsel Ethics Counsel OK Question Title * 7. FAIR Federal Assessment of Institutional Research Federal Award for Investigational Research Findable, Accessible, Interoperable, Reusable OK Question Title * 8. GDP General Device Protocol Good Documentation Practice Good Device Practices OK Question Title * 9. HIPAA Health Insurance Portability and Accountability Act Health Insurance Protection and Accessibility Act Health Institute for Patient Accessibility and Accommodation OK Question Title * 10. IDE International Device Exemptions Investigational Device Exemptions International Data Ethics OK Question Title * 11. LRAA Library of Regulatory Affairs Administration Local Regulatory Affairs Associate Local Research Administrative Associate OK Question Title * 12. MCA Medicare Clinical Analysis Medical Coverage Act Medicare Coverage Analysis OK Question Title * 13. NDA New Drug Assessment New Drug Application National Device Association OK Question Title * 14. OSR Outside Safety Report Outside Safety Review Office of Science and Research OK Question Title * 15. PC Protocol Committee Protocol Coordinator Protected Conditions OK Question Title * 16. QCT Quality Clinical Trials Qualifying Clinical Terminology Qualifying Clinical Trial OK Question Title * 17. SDR Source Data Review Site Data Review Source Document Review OK Question Title * 18. SRB Science and Research Board Site Review Board Scientific Review Board OK Question Title * 19. TMF Trial Master File Terminated Master File Trial Management Files OK Question Title * 20. UADE United Affiliates for Device Efficiency Unanticipated Adverse Device Effect Unanticipated Adverse Drug Event OK DONE