Registrar
Assistance with U.S. FDA Regulations
The U.S. Food and Drug Administration (FDA) now requires medical device manufacturers and importers to submit mandatory initial and supplemental adverse event reports in electronic format through FDA’s Electronic Submission Gateway (ESG). Registrar Corp can help submit your reports in eMDR format.
For assistance, simply complete the form below:
The U.S. Food and Drug Administration (FDA) requires that all registered food, medical device, and drug facilities renew their FDA registration between October 1 and December 31,
The U.S. FDA Registration Renewal period CLOSED on December 31,
If you did not renew by the deadline, you must re-register with FDA.
Re-register or verify that your registration was renewed for :
Get 18 Months of Registration and U.S. Agent service for the price of 12 when you sign up today.