Galit Berler Sr. QA Conultant, HaMaDa
Join Our Expert-Led Webinar and Gain Crucial Insights on:
- FDA announcement
- Change background
- Change interpretation and implications
- New 21 CFR part 820 structure
- FDA QMSR vs. ISO13485 requirements
- Change implementation plan
Galit Berler, Sr. QA consultant, expert in QA management and implementation, more than 16 years of experience in the medical device industry
- 21.07.25 Monday
- 14:00-15:00
Contact Us For Recording
הוובינר הזה כבר נערך, כדי לקבל קישור לצפייה בוובינר המוקלט אנא “צור קשר” ובקש הקלטה מס’ 105.
This Webinar was already held, to receive a link to watch the recorded Webinar please contact us and ask for recording No.#105.