Medical Innovation Exchange

premarket approval

Final Guidance for Submission of Off-The-Shelf Software in Medical Devices

Final Guidance for Submission of Off-The-Shelf Software in Medical Devices     On August 11, the FDA released the Final Guidance Off-the-Shelf Software Use in Medical Devices. The document, which supersedes Off-The-Shelf Software Use in Medical Devices issued September 27, 2019, provides information on recommended documentation sponsors should include in a premarket submission for FDA’s evaluation …

Final Guidance for Submission of Off-The-Shelf Software in Medical Devices Read More »

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks     From cybsecurity to remote inspections, recalls and quality management, medical technology regulations are rapidly expanding. This increase in global regulatory demands has presented new challenges for regulatory affairs and intelligence teams. On May 16-17, The MedTech Regulatory Intelligence Summit will bring together regulatory …

MedTech Regulatory Compliance: Join the Discussion and Expand Your Regulatory Networks Read More »