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BioWorld - Sunday, February 15, 2026
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Home » Implementation times a key concern for industry in FDA harmonization draft
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Implementation times a key concern for industry in FDA harmonization draft

March 2, 2022
By Mark McCarty
The FDA’s proposal to harmonize the Quality System Regulation (QSR) with ISO 13485 has finally become more than just a hot topic among device makers, and the agency held a March 2 advisory hearing on the matter. One of the critical concerns for industry is the proposal of a one-year term of implementation upon publication of a final harmonization rule, a timeline that some argue should be doubled or tripled in order to serve as a practicable implementation timeline.
Medical technology Regulatory U.S. FDA

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