FY 2025 OMUFA Fees Due June 2: What You Need to Know
FDA’s FY 2025 OMUFA fees are due June 22 for OTC drug manufacturers and contract facilities. Learn what this means and how to stay compliant.
... Read more June 1, 2025
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[blog_list]
FDA to Revoke Use of Red No. 3: What You Need to Know
Find out why the FDA is banning Red No. 3 in food and ingested drugs. Understand the impact and compliance updates.
... Read more January 17, 2025
What’s Behind the FDA’s New Front-of-Package Labeling Proposal?
The FDA’s proposed front-of-package (FOP) nutrition labeling rule introduces significant changes to how nutritional information is displayed. This proposal reflects
... Read more January 16, 2025
The Role of FDA Agents in U.S. Compliance
In a world where the pharmaceutical industry is constantly evolving and new drugs are being introduced to the market every
... Read more June 28, 2023
Managing FDA Fees: Budgeting and Planning for Success
Are you a company in the healthcare or pharmaceutical industry looking to bring a new product to market? If so,
... Read more June 16, 2023
Inside Scoop FDA Medical Device User Fees (MDUFA) for 2023
The FDA or U.S. Food and Drug Administration recently announced the Fiscal Year Medical Device User Fee (MDUFA) amendments. The
... Read more November 1, 2022
FDA Releases Draft Guidance on Enforcement Discretion for Certain NAC Products
Navigating the FDA and NAC regulations can be intimidating, but with the right information and guidance, you’ll be able to
... Read more August 4, 2022