Home > Newsletters > International Medical Device Regulatory Monitor > Presubmissions Draft Guidance Due Soon, Industry Best Practice Paves Way for Now
International Medical Device Regulatory Monitor
April 2012 | Vol. 20 No. 4
Presubmissions Draft Guidance Due Soon, Industry Best Practice Paves Way for Now
A new draft guidance outlining expectations for presubmission meetings with the U.S. Food and Drug Administration (FDA) is expected in the next few months, regulators said during a March 5 Regulatory Affairs Professionals Society meeting.
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