Under 21 CFR 1.232(a)(6), you must provide the email address of the owner, operator, or agent
in charge of the facility unless FDA has granted a waiver from such requirement. In addition,
under 21 CFR 1.230(b) and (c), 1.232(a)(10), 1.234(a), and 1.235(b)(5), registration renewals,
abbreviated registration renewals, registrations, updates, and cancellations not submitted by the
owner, operator, or agent in charge must include the email address for the individual who
authorized the submission, unless FDA has granted a waiver under 21 CFR 1.245.
If you are submitting a waiver from the email requirement, you must submit a written request to
FDA that explains why it is not reasonable for you to submit the required email address
information (21 CFR 1.245).