Complying with MoCRA:

New FDA Cosmetics Regulation

Recorded Wednesday, September 27, 2023

FDA has recently released draft guidance on the Modernization of Cosmetics Act of 2022, commonly known as MoCRA. This guidance addresses the first of many compliance requirements for industry—cosmetic product facility registration and listing. The first submission deadline relating to MoCRA is right around the corner, on December 29, 2023. To help industry prepare for this upcoming deadline, Reed Tech will be hosting a free, educational webinar presented by Reed Tech and Garg Law.

This webinar, recorded Wednesday, September 27th, is a high-level overview of MoCRA and its implications for cosmetics manufacturers, processors and responsible persons presented by subject-matter experts Caitlin Lynes, Strategic Account Manager, Reed Tech and Shelly Garg, President and Founder, Garg Law, a full-service FDA regulatory law firm. This webinar provides industry with an understanding of key requirements and necessary preparation for MoCRA compliance.

Key Topics:

  • MoCRA Overview
  • Compliance Requirements and Exemptions
  • Compliance Preparation
  • Expected Regulation Implementation 

For more information about MoCRA, visit our resource pages: Reed Tech and Garg Law.


Caitlin Lynes (002)

Caitlin Lynes,  Reed Tech

Shelly Garg (2)

Shelly Garg, Garg Law

 More questions? Contact or +1-215-557-3010.

About LexisNexis Reed Tech

LexisNexis Reed Tech brings clarity to innovation for businesses worldwide. We enable innovators to accomplish more by helping them make informed decisions, be more productive, comply with regulations, and ultimately achieve a competitive advantage for their business. Our Reed Tech suite of SingleSource™️ for Medical Devices, SingleSource™️ for Drug Products, and Navigator™️ for Drug Labels enables life sciences companies to create product data management strategies and meet compliance deadlines on time. We are proud to directly support and serve these innovators in their endeavors to better humankind.

For more information, please visit


About Garg Law

Garg Law is a full-service FDA regulatory law firm that provides advice, counsel, and ongoing support on FDA product compliance and enforcement. The firm provides strategic advice on complying with FDA requirements for food, beverage, dietary supplement, cosmetic, drug and device companies, through the product’s lifecycle beginning from product development, launch, and post-launch compliance.

The firm also provides strategic counsel on overlapping agency requirements, including those of U.S. Customs and Border Protection, U.S. Department of Agriculture, Environmental Protection Agency, Alcohol Tax and Trade Bureau, and the Consumer Product Safety Commission.

Garg law’s focus is to enhance product value, ensure product and regulatory compliance, and help companies make decisions to mitigate costly and time-consuming regulatory scrutiny, adverse public reaction, and business disruption with professionalism, value and a dedication to excellence.

For more information, please visit Garg Law.

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