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The United States FDA regulates products intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease or intended to affect the structure or any function of the body of man or other animals. Registrar Corp provides Registration, Update, and Renewal assistance for U.S. and Non-U.S. companies in the Drug industry.

If already registered with FDA
Click here	As of June 2009, drug registrations, listings, annual renewals and updates must be submitted to FDA electronically. Drug labels must be indexed using extensible markup language (XML) in SPL format. To register or renew, drug establishments must provide DUNS numbers for their private label distributors, manufacturers and importers. The new requirements apply to Over-the-Counter Drugs, Active Pharmaceutical Ingredients, Prescription Drugs, Homeopathic Drugs, and Animal Drug Products. Registrar Corp can assist you to quickly and easily transition to FDA's new electronic drug system.

If not yet registered with FDA
Click here	Registrar Corp can assist with registrations, listings, U.S. Agent requirement, and Drug label submissions.

Applicable U.S. Regulations:

FDA Regulation: 21 C.F.R. Part 207

Registrar Corp assists businesses with FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling FDA registration requirements. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the US Food and Drug Administration.


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