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POST ID: 5720

Webinar On Best Practices for 510(k) Drafting and Submission: Dos and Don'ts

Region: Canada
Location: Mississauga, ON


From this webinar you will learn best practices for adequately putting your 510(k) together for your successful submission to the FDA, compliant with the FDA’s eCopy and RTA policy.
This session will greatly help you streamline your 510(k) preparation and submission process at your firm for maximum benefits in a least burdensome, effective manner.
David will share his PASS-IT solutions based on what he has learned from his own experience including his recent analysis of various different types of 510(k)s that have been recently cleared.
This session is a must for regulatory professionals working in medical device industry including those who are interested in the topic.

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