CDRH New Update

CDRHNew

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and Device Manufacturer Communications With Payors, Formulary Committees, and Similar Entities--Questions and Answers; Draft Guidance for Industry and Review Staff; Availability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Communications That Are Consistent With the Food and Drug Administration-Required Labeling--Questions and Answers; Draft Guidance for Industry; Availability