In a Westlaw Today article, life sciences regulatory & compliance partner Joshua Oyster and associate Austin Laroche analyzed 10 ey points to consider in planning how to comply with the U.S. Food and Drug Administration's final rule amending the current good manufacturing practice requirements for medical devices.
The authors summarize their top 10 takeaways for medical device industry stakeholders to consider as they plan for compliance with the new FDA Quality Management System Regulation.
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