June Workshop Will Cover CDRH Guidance Development

The FDA’s Center for Devices and Radiological Health is planning a June 5 public workshop to share information about its guidance development process and seek feedback from stakeholders. The aim is to advance collaborative efforts on guidance development by the center and device industry.

Participants will discuss CDRH’s guidance priorities and priority development, as well as best practices for CDRH and its stakeholders. The workshop will also include information about development and practical implementation of the internal guidance development process, according to a notice in today’s Federal Register.

The workshop will take place at the FDA’s White Oak campus in Silver Spring, Md.

Interested parties may submit comments on the discussion topics to docket no. FDA-2014-N-0530 at regulations.gov  through July 7. The deadline to register for the workshop and/or view the webcast is May 29. — Lena Freund

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