Prepping for a MoCRA and FDA Cosmetics Inspection In a recent News & Insights publication, we addressed FDA’s significant inspection increase, including top citations for
FDA Announces New Medical Device User Fees for FY 2024 FDA announced its update on medical device user fees for FY 2024, which runs October
What You Need to Have in Place Now for MoCRA Cosmetic Product Substantiation While FDA cosmetic product safety has always been required, MoCRA ups the
Today, FDA issued long-awaited draft guidance on cosmetic facility registrations and product listings, as required under the Modernization of Cosmetics Act Regulation of 2022 (MoCRA).
Are you considering starting your own cosmetic product manufacturing facility? To ensure successful production and compliance with industry standards, it’s crucial to understand the specific
Cosmetic Facility Registration, Product Listing, Record-Keeping, Recall Readiness, and Labeling and Substantiation Compliance for Lasting Radiance Hear ye hear ye! Implementation deadlines and compliance dates
A Look at FDA’s Regulation of Sunscreen FDA has regulated sunscreen since the 1970s to ensure that consumers have access to safe and effective sun
This week, FDA kicked-off a new resource about the Modernization of Cosmetics Regulation Act of 2002 (MoCRA) and a follow-up constituent advisory that FDA has
Marketing Sunglasses, Bandages, Hospital Equipment, Pregnancy Test Kits, Cosmetic Devices, Personal Lubricants and More The U.S. leads the world in medical innovation and is the
Protecting Consumers, Limiting Supply Chain Disruption and Avoiding Business and Reputation Damage Quickly and Effectively With product recalls consistently being in the news over undeclared
