This article presents a strategy that benefits medical device manufacturers who initiate risk management early in the product development lifecycle. A risk management program compliant to the latest revisions of ISO14971, can support design, verification, validation efforts, improve post-market planning, and simplify regulatory compliance. Find out how.

This article presents a strategy that medical device manufacturers can use to assess, analyze, and control risks related to the use of medical devices, compliant to the latest revisions of ISO14971.