REGISTER TODAY!
Both experts and those entering into the regulatory industry will benefit from this event.
3 key reasons to attend this event:
1. Gain a Foundational and Practical Understanding of the Pre-Sub Program: You will learn what the FDA Pre-submission (Pre-Sub) program is, and more importantly, how and when to use it most effectively for your specific device development pathway.
2. Learn Expert Strategies for Successful Navigation: The session offers practical tips from industry experts who have been successfully using the program since its inception. The information includes crucial guidance on how to truly listen to what the FDA is saying (or not saying).
3. Master Disagreement Resolution: You will learn practical strategies for how to handle inevitable disagreements with the FDA, which is a critical skill for keeping your development timeline on track.
REGISTRATION: Member: $20 |Nonmember: $40 | Student Members $0 | Student Nonmembers $0 (With Promo Code)
*Please reach out to a RAPS Twin Cities Chapter Leader to request a Student Promo Code
LinkedIn
https://my.raps.org/events/event-registration/?id=9673143a-b389-f011-8150-7c1e5295eaaa&_gl=1*71xhk*_gcl_au*MTEzMDI5Nzk1Ny4xNzYyOTgwODg5*_ga*MTU1MjA3MTI2Mi4xNzU1MDkxNTA0*_ga_42DFN1C8P8*czE3NjI5ODA4OTAkbzUkZzEkdDE3NjI5ODE0NDgkajYwJGwwJGgw
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Georgiann Keyport MSc, RAC, FRAPS
Senior Advisor, Principal Regulatory, Quality and Clinical Affairs Consultant, Adjunct Professor
Canopy Regulatory Solutions Inc.
Chaska MN
United States
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