CDRHNew
Date: November 1, 2013
The following new items were added to the CDRH web pages on October 31, 2013. Previous CDRH New Items can be found on the CDRHNew Page.
- Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Electronic Products
- Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance on Medical Devices: The Pre-Submission Program and Meetings With FDA Staff
- Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Approval of Medical Devices
- FDA/American Gastroenterological Association (AGA) Co-sponsored Public Workshop: Changing Regulatory and Reimbursement Paradigms for Medical Devices in the Treatment of Obesity and Metabolic Diseases, December 19-20, 2013
- CDRHLearn Presentation: International Medical Device Regulators Forum (IMDRF) Medical Device Single Audit Program (MDSAP) Pilot
| This email was sent to kostikblog@ukr.net using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 800-439-1420 |  |
