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21 CFR 1317.40

§ 1317.40 Registrants authorized to collect and authorized collection activities.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 1317.40, § 1317.40 Registrants authorized to collect and authorized collection activities, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/92289
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Full text

(a) Manufacturers, distributors, reverse distributors, narcotic treatment programs, hospitals/clinics with an on-site pharmacy, and retail pharmacies that desire to be collectors shall modify their registration to obtain authorization to be a collector in accordance with § 1301.51 of this chapter. Authorization to be a collector is subject to renewal. If a registrant that is authorized to collect ceases activities as a collector, such registrant shall notify the Administration in accordance with § 1301.52(f) of this chapter. (b) Collection by registrants shall occur only at the following locations: (1) Those registered locations of manufacturers, distributors, reverse distributors, narcotic treatment programs, hospitals/clinics with an on-site pharmacy, and retail pharmacies that are authorized for collection; and (2) Long-term care facilities at which registered hospitals/clinics or retail pharmacies are authorized to maintain collection receptacles. (c) Collectors may conduct the following activities: (1) Receive and destroy mail-back packages pursuant to § 1317.70 at an authorized registered location that has an on-site method of destruction; (2) Install, manage, and maintain collection receptacles located at their authorized collection location(s) pursuant to §§ 1317.75 and 1317.80; and (3) Promptly dispose of sealed inner liners and their contents as provided for in § 1317.05(c)(2).

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.