FY 2025 OMUFA Fees Due June 2: What You Need to Know
The FDA has confirmed that FY 2025 OMUFA facility fees are due soon. If your business was registered as a
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June 1, 2025
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[blog_list]
FDA to Revoke Use of Red No. 3: What You Need to Know
The FDA has just announced a significant decision: Red No. 3, a widely used synthetic dye in foods and ingested
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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
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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
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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,
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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
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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FDA Releases Draft Guidance on Enforcement Discretion for Certain NAC Products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
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August 4, 2022