Adverse Event Reporting System (FAERS) 7
- Use of Real-World Data to Generate Evidence for Medical Device Regulatory Decisions
- Benefit-Risk Factors in Medical Device Product Availability, Compliance, and Enforcement Decisions
- Medical Device Reporting (MDR) Requirements and Procedures for Manufacturers
- Labeling Requirements for Permanent Hysteroscopic Tubal Implants for Female Sterilization
- Electronic Medical Device Reporting: Questions and Answers on Electronic Submission of Postmarket Reports
- Medical Device Reporting for Needlestick and Other Sharps Injuries
- Medical Device Reporting: Manufacturer Report Number Format Variances