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Blog

NAFTA and the FDA

The North American Free Trade Agreement (NAFTA) assists with protecting the Food and Drug Administration (FDA) of the United States’ right to guarantee food safety and consistency within North America. Implemented on January 1, 1994, the agreement involves Canada, the United States, and Mexico and is meant to expand the scope of free trade and […]

Useful Information on FDA Certificate of Registration

Companies that manufacture goods subject to U.S. Food and Drug Administration (FDA) regulation are required to declare their facilities with the FDA. The FDA provides identification numbers upon active registration, but it stops short of providing Certificates of Registration. Even so, often purchasers or importers seek proof of their registration from vendors. UReg FDA Registrations […]

Common FDA Inspection Violations

Part of maintaining FDA compliance is ensuring that you’re taking all of the necessary precautions and steps to be compliant in the event of an FDA inspection. Where others have run into violation issues, you can avoid making these same mistakes by being aware of some of the most common violations and employing the steps […]

FDA UDIs: How Many Will You Need?

Before we get to the primary topic, you should know that the United States FDA Registration Renewal period closed on December 31, 2020. If your renewal was not processed by the deadline, you are required to go through the FDA re-registration process. Today, we’d like to briefly talk about the number of FDA Unique Device […]