21 CFR (FDA) and (EU) MDR Standards
This webinar takes a "birds-eye-view" of what the different parts of 21 CFR are, as they apply to Medical Device Manufacturing, and also looking at the corresponding articles of (EU) MDR. We'll not only discuss similarities but also touch on some of the differences.
There are various standards within the Medical Device Sector of the industry that lie outside of statutory regulations but are extremely important, and if not followed will cause havoc in meeting regulations. What are they and where can they be found? If you are not a "regulatory guru", but have an interest in knowing about the regulations, attending this short webinar, will be an excellent way of getting your feet wet in the regulatory world, without drowning in the details.
Watch this Webinar to understand 21 CFR (FDA) and (EU) MDR Standards in detail.
Upcoming Webinar : Countdown to Compliance: Understanding the CMMC 2.0 Rollout
Speakers:
Date and Time:
Oct 9 2025 11:00AM Eastern Time (US and Canada)
RegisterUpcoming Webinar : De la Teoría a la Práctica: Interpretando GD&T en la Industria Automotriz
Speakers:
Julio Rodriguez
Date and Time:
Oct 14 2025 10:00AM Mexico City
RegisterUpcoming Webinar : California’s climate disclosure rules target companies nationwide
Speakers:
Date and Time:
Oct 16 2025 11:00AM Eastern Time (US and Canada)
RegisterUpcoming Webinar : Why NADCAP Matters: Ensuring Quality in Aerospace Manufacturing
Speakers:
stephen Hall
Date and Time:
Oct 21 2025 11:00AM Eastern Time (US and Canada)
RegisterUpcoming Webinar : Updates on IATF 16949, IA 9100, ISO 13485, and ISO 23485
Speakers:
Chad Kymal, Frankie Breedlove, William kovacich
Date and Time:
Oct 28 2025 11:00AM Eastern Time (US and Canada)
Register