Date: January 23, 2017
The following new items were added to the CDRH web pages on January 19, 2017. Previous CDRH New Items can be found on the CDRHNew Page.
- Federal Register: Agency Information Collection Activities; Proposed Collection; Comment Request; Adverse Event Program for Medical Devices (Medical Product Safety Network)
- Federal Register: Drug and Device Manufacturer Communications With Payors, Formulary Committees, and Similar Entities--Questions and Answers; Draft Guidance for Industry and Review Staff; Availability
- Federal Register: Manufacturer Communications Regarding Unapproved Uses of Approved or Cleared Medical Products; Availability of Memorandum; Reopening of the Comment Period
- Federal Register: Medical Product Communications That Are Consistent With the Food and Drug Administration-Required Labeling--Questions and Answers; Draft Guidance for Industry; Availability