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Home » Part 806 Reports — When to Submit Them and How to Avoid Pitfalls
Part 806 Reports — When to Submit Them and How to Avoid Pitfalls
Covington & Burling attorney Pamela Forrest offered insights into when devicemakers must file recall reports with the FDA to comply with 21 CFR Part 806 in a recent FDAnews webinar, flagging areas of confusion and how to avoid common errors.