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|---|---|---|
 Clinical research Clinical Data Management Food and Drug Administration Drug safety Electronic Common Technical Document Health Level 7 Prescription Drug User Fee Act Medical device Regulated Product Submissions Medicine Health Medical informatics |
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Microsoft PowerPoint - 281_Gray.ppt [Compatibility Mode] | Regulated Product Submissions (RPS) Nancy Shadeed DITTA Workshop on RPS March 23, 2015DocID: 1eXev - View Document |
| IMDRF Table of Contents (ToC) Pilot PlanDocID: 11D6b - View Document |
| IMDRF/RPS WG/N26FINAL:2015DocID: W7Sv - View Document |
| Proposed document: Assembly and Technical Guide for IMDRF Table of Contents (ToC) Submissions (ToC-based submissions)DocID: W45m - View Document |
| How FDA validates reported suspect products in adverse event reports submitted to FAERSDocID: JP2X - View Document |