Why is Ferrosa more professional?
Customer Case Studies
FDA registration success stories
We have successfully helped food, cosmetics, and pharmaceutical companies complete FDA registration. Some client cases are shown below:
DSC Successfully Completes Dun & Bradstreet Code Application and FDA Food Registration
Shiyin Medical Endoscope US Agent Service
Jiatai Laser Equipment Radiation Electronics FDA Registration
Anhui Lu Mama Biotechnology Co., Ltd. Dental Floss Medical Device Registration
Guangzhou Jianyuan Biotechnology Pharmaceutical Enterprise Registration and NDC Registration
Winona Cosmetics Successfully Completes Corporate and Product Registration
News / Industry Information
FDA Registration Information and Latest Updates
Stay updated on the latest FDA registration policies, industry trends, and compliance guidelines. Learn about the registration processes and considerations for food, cosmetics, pharmaceuticals, medical devices, and radiation-emitting electronic products. Ferosha provides expert interpretations and practical information to help businesses stay informed about regulatory changes and successfully conduct business in the US market.
Good news! The FDA has announced the Over-the-Counter (OTC) Drug Monograph Facility Fee for Fiscal Year 2026, with fees nearly halved!
2024-2025 Cosmetics Company Registration Service Summary
How can Yunnan's foreign trade enterprises leverage government subsidies to efficiently complete US FDA registration?
2025 Annual Summary of Registration Services for Pharmaceutical and Medical Device Enterprises
The FDA will fully resume normal operations.
📢 Background: Risk of US Government Shutdown Averted. Recently, the US Senate completed a series of key votes, officially passing the Continuing Appropriations and Extensions Act. ...
FDA FY 2026 Funding Lapse: Key Considerations for Companies and Industries
Background: According to the FDA's official website, if during the period between October 1, 2025, and before the FY 2026 appropriations are passed or a Continuing Resolution is passed (i.e., the “lapse period”), the FDA...
