FALLS CHURCH, Va., August 13, 2019 /PRNewswire-PRWeb/ -- Preparing for a MDSAP Audit A Case Study from the Manufacturer's
Devicemakers selling into Canada, Japan, Australia or Brazil, listen up: There is a new audit regime.
It's called the Medical Device Single Audit Program (MDSAP), and Canada began imposing it on every imported medical device as of Jan. 1, 2019. The three other nations will follow shortly.
FDA and ISO device inspections and audits will change too. The U.S. is a member of the five-nation compact that agreed to the new audit protocols.
Mark the calendar for Tuesday, Aug. 27, when consultant Connie Hoy walks attendees through this unfamiliar audit territory. Over the course of 90 fast-paced minutes, attendees will discover best practices for:
Interested in registering multiple sites? Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally to learn about our special multisite discount.
Webinar Details: Preparing for a MDSAP Audit A Case Study from the Manufacturer's Perspective An FDAnews Webinar Tuesday, Aug. 27, 2018 1:30 p.m.-3:00 p.m. EDT https://www.fdanews.com/preparingforamdsapauditcase
Tuition: $287 per site
Easy Ways to Register: Online: https://www.fdanews.com/preparingforamdsapauditcase By phone: 888-838-5578 or 703-538-7600
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