US FDA to hold forum for experienced regulators

摘要

The US Food and Drug Administration's devices centre plans to hold a meeting in September; where it will be able to exchange regulatory information with its counterpart agencies from around the world'.The FDA's Center for Devices and Radiological Health Forum for International Medical Device Regulatory Authorities, scheduled for 13-15 September; is aimed at experienced regulatory authorities and is not open to the general public.CDRH notes that this forum is an advanced session; it held a similar forum in May, which was open to less experienced authorities and provided information about the US medical device regulatory processes, and explained the role of CDRH as well as the science, technology, regulations and processes it uses.