FALLS CHURCH, Va., Oct. 4, 2019 /PRNewswire-PRWeb/ -- Medical Device Nonconforming Audit Findings Corrective Action That's
Despite best efforts to the contrary, getting nonconformities from a notified body during an audit does happen. How best to respond?
Organizations will be under a strict deadline… under pressure … to find out the corrective plan isn't right.
There are better ways to address these nonconformities, and an expert with over three decades of experience in the medical device industry — Connie Hoy, founder of Hoy & Associates Regulatory Consulting — is here to explain them in this informative webinar.
Using real-life examples that show appropriate versus inappropriate responses, Ms. Hoy will share how to:
If one might be tasked with responding to a regulatory audit — or signing a name to one — this webinar is a must.
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: Medical Device Nonconforming Audit Findings Corrective Action That's Right for Your Company An FDAnews Webinar Tuesday, Oct. 15, 2019, 1:30-3:00 p.m. EDT https://www.fdanews.com/mdnonaudit
Tuition: $287 per site
Easy Ways to Register: Online: https://www.fdanews.com/mdnonaudit By phone: 888-838-5578 or 703-538-7600
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