FDA is providing an abbreviated registration renewal process for facilities that do not have
information changes under 21 CFR 1.232 since the submission of the preceding registration,
registration renewal, or update (see 21 CFR 1.230(c)).
If you use the abbreviated registration renewal process, you must confirm that no changes have
been made to the information required under 21 CFR 1.232 since you submitted the preceding
registration, registration renewal, or update, and you must certify that the information submitted
is truthful and accurate. Each electronic abbreviated registration renewal must include the name
of the individual submitting the abbreviated renewal. For registrations submitted by mail or fax,
each abbreviated registration renewal must also include the individual’s signature (see 21 CFR
1.230(c)).
For abbreviated registration renewals not submitted by the owner, operator, or agent in charge of
the facility, the abbreviated renewal must provide the email address of the individual who
authorized submission of the abbreviated renewal, unless FDA has granted a waiver under 21
CFR 1.245 (21 CFR 1.230(c)).
