Home » Expert: Document Production Essential Part of Inspections
Expert: Document Production Essential Part of Inspections
FDA investigators are cracking down on devicemakers that are not able to produce documents during inspections, Elizabeth Troll, a 25-year veteran of the
industry, said at a recent FDAnews webinar. The opportunity to get a second chance to correct observations from inspections is more limited now, she said,
because investigators have been clear in their expectations.
The GMP Letter
The GMP Letter
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