21CFR1.1380

(a) In general, the procedures set forth in § 10.30 of this chapter govern FDA's response to a petition requesting modified requirements or an exemption. An interested person may submit comments on such a petition in accordance with § 10.30(d) of this chapter . (b) Under § 10.30(h)(3) of this chapter , FDA will publish a notice in the Federal Register requesting information and views on a submitted petition, including information and views from persons who could be affected by the modified requirements or exemption if we granted the petition. (c) Under § 10.30(e)(3) of this chapter , we will respond to the petitioner in writing, as follows: (d) We will make readily accessible to the public, and periodically update, a list of petitions requesting modified requirements or exemptions, including the status of each petition (for example, pending, granted, or denied). (1) If we grant the petition either in whole or in part, we will publish a notice in the Federal Register setting forth any modified requirements or exemptions and the reasons for them. (2) If we deny the petition (including a partial denial), our written response to the petitioner will explain the reasons for the denial.