Top Industry News
- FDA- Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices
- MHLW Pharmaceuticals and Medical Devices Safety Information (FY2017)
- E-Submissions of REMS Documents: FDA Offers Draft Guidance
- FDA Finalizes Guidance on Deviation Reporting for HCT/Ps
- FDA Wants to Know What Regulations and Paperwork Requirements Need to Go
- Expedited Approval Pathways Associated With Increased Safety-Related Label Changes, Study Finds