HHS - 21 CFR PART 16
REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
| Organization: | HHS |
| Publication Date: | 1 April 2018 |
| Status: | active |
| Page Count: | 8 |
scope:
The procedures in this part apply when: (a) The Commissioner is considering any regulatory action, including a refusal to act, and concludes, as a matter of discretion, on the Commissioner's initiative or at the suggestion of any person, to offer an opportunity for a regulatory hearing to obtain additional information before making a decision or taking action.
(b) The act or a regulation provides a person with an opportunity for a hearing on a regulatory action, including proposed action, and the act or a regulation either specifically provides an opportunity for a regulatory hearing under this part or provides an opportunity for a hearing for which no procedures are specified by regulation. Listed below are the statutory and regulatory provisions under which regulatory hearings are available:
(1) Statutory provisions: Section 304(g) of the act relating to the administrative detention of devices and drugs (see §§ 800.55(g) and 1.980(g) of this chapter). Section 304(h) of the act relating to the administrative detention of food for human or animal consumption (see part 1, subpart k of this chapter). Section 419(c)(2)(D) of the Federal Food, Drug, and Cosmetic Act relating to the modification or revocation of a variance from the requirements of section 419 (see part 112, subpart P of this chapter).
Document History