[both parts now live!] MoCRA in Action: Current Status, Pitfalls and New Insights — Free Two-part Digital Roundtable

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On-demand access is now available! Register below to watch.
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The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is in the initial stages of implementation. The first step, including facility registrations and product listings, was enacted on July 1, 2024, after a six-month delay to allow the industry to better prepare.

Register now to watch the digital roundtable - Part I and Part II are now available on demand!

Now that MoCRA is in action, it is putting those preparations to the test — and there are early indicators that companies are facing challenges; for example, preparing for adverse event reporting and formalizing "handshake agreements."

The good news is the U.S. Food and Drug Administration (FDA) is willing to work with the industry to help navigate and resolve these issues, according to the panelists in our latest two-part Digital Roundtable discussion, sponsored by NSF.

Part I, MoCRA in Action

Now available on demand, "MoCRA in Action: Current Status, Pitfalls and New Insights, Part I," gives a pulse on:

  • The current status of MoCRA's implementation;
  • Milestone deadlines on the horizon;
  • How well companies and the FDA are handling MoCRA's implementation; and
  • The biggest pitfalls/challenges for companies — and ways to avoid them.

REGISTER HERE for on-demand access to Part I. Already registered? Click through to watch now.

Part II, MoCRA in Action

Part II is now live and explores:

  • The less obvious impact(s), especially for larger companies;
  • How MoCRA is affecting day-to-day product development;
  • Feedback from the industry about what MoCRA missed;
  • And more.

REGISTER HERE for on-demand access to Part II. Already registered? Click through to watch now.

MoCRA Digital Roundtable Panelist Lineup

Featured panelists include:
  • Harold Chase, Director of Government Affairs, NSF
  • John Misock, Senior Consultant at Ceutical Laboratories and former FDA regulatory microbiologist
  • Ken Stevenson, VP of Regulatory Affairs, Ceutical Laboratories
  • Jaclyn Bellomo, Director of Cosmetics Services and Software, Registrar Corp. and
  • Meredith Petillo, VP of Technical and Regulatory Affairs, Independent Beauty Association

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