FDA Webinar Final MDR guidance

On November 30, 2016 FDA held a Webinar – Final Guidance on Medical Device Reporting for Manufacturers – November 30, 2016 The full presentation materials and a transcript are at the link provided.

CSV Training Course

Learn FDA expectations for software validation for computer systems, quality system software, manufacturing and production process software, and engineering tools. Email training@softwarecpr.com for more info.

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