FDA to Hold Public Meeting in June on Regulatory Guidance for Medical Devices

The Food and Drug Administration will hold a workshop June 5 in Silver Spring, Md. to discuss the guidance development process for medical devices. At the meeting, FDA will discuss with the public best practices in guidance development, as well as how the agency’s Center for Devices and Radiological Health should develop its guidance priorities. Registration is required by May 29 to attend the meeting in person or watch the meeting via webcast.