21 C.F.R. Subpart B—Procedures for Registration and Listing
Title 21 - Food and Drugs
(a) You must register and submit a list of every HCT/P that your establishment manufactures within 5 days after beginning operations or within 30 days of the effective date of this regulation, whichever is later. (b) You must update your establishment registration annually in December, except as required by §1271.26. You may accomplish your annual registration in conjunction with updating your HCT/P list under paragraph (c) of this section. (c)(i) If no change described in §1271.25(c) has occurred since you previously submitted an HCT/P list, you are not required to update your listing. (ii) If a change described in §1271.25(c) has occurred, you must update your HCT/P listing with the new information: (a) At the time of the change, or (b) Each June or December, whichever month occurs first after the change. [69 FR 68681, Nov. 24, 2004] (a) Your establishment registration Form FDA 3356 must include: (1) The legal name(s) of the establishment; (2) Each location, including the street address of the establishment and the postal service zip code; (3) The name, address, and title of the reporting official; and (4) A dated signature by the reporting official affirming that all information contained in the establishment registration and HCT/P listing form is true and accurate, to the best of his or her knowledge. (b) Your HCT/P listing must include all HCT/P's (including the established name and the proprietary name) that you recover, process, store, label, package, distribute, or for which you perform donor screening or testing. You must also state whether each HCT/P meets the criteria set out in §1271.10. (c) Your HCT/P listing update must include: (1) A list of each HCT/P that you have begun recovering, processing, storing, labeling, packaging, distributing, or for which you have begun donor screening or testing, that has not been included in any list previously submitted. You must provide all of the information required by §1271.25(b) for each new HCT/P. (2) A list of each HCT/P formerly listed in accordance with §1271.21(a) for which you have discontinued recovery, processing, storage, labeling, packaging, distribution, or donor screening or testing, including for each HCT/P so listed, the identity by established name and proprietary name, and the date of discontinuance. We request but do not require that you include the reason for discontinuance with this information. (3) A list of each HCT/P for which a notice of discontinuance was submitted under paragraph (c)(2) of this section and for which you have resumed recovery, processing, storage, labeling, packaging, distribution, or donor screening or testing, including the identity by established name and proprietary name, the date of resumption, and any other information required by §1271.25(b) not previously submitted. (4) Any material change in any information previously submitted. Material changes include any change in information submitted on Form FDA 3356, such as whether the HCT/P meets the criteria set out in §1271.10. If the ownership or location of your establishment changes, you must submit an amendment to registration within 5 days of the change. (a) FDA will assign each location a permanent registration number. (b) FDA acceptance of an establishment registration and HCT/P listing form does not constitute a determination that an establishment is in compliance with applicable rules and regulations or that the HCT/P is licensed or approved by FDA. (a) A copy of the Form FDA 3356 filed by each establishment will be available for public inspection at the Office of Communication, Training, and Manufacturers Assistance (HFM–48), Center for Biologics Evaluation and Research, Food and Drug Administration, 1401 Rockville Pike, suite 200N, Rockville, MD 20852–1448. In addition, there will be available for inspection at each of the Food and Drug Administration district offices the same information for firms within the geographical area of such district office. Upon request and receipt of a self-addressed stamped envelope, verification of a registration number or the location of a registered establishment will be provided. The following information submitted under the HCT/P requirements is illustrative of the type of information that will be available for public disclosure when it is compiled: (1) A list of all HCT/P's; (2) A list of all HCT/P's manufactured by each establishment; (3) A list of all HCT/P's discontinued; and (4) All data or information that has already become a matter of public record. (b) You should direct your requests for information regarding HCT/P establishment registrations and HCT/P listings to the Office of Communication, Training and Manufacturers Assistance (HFM–48), Center for Biologics Evaluation and Research, Food and Drug Administration, 1401 Rockville Pike, suite 200N, Rockville, MD 20852–1448.
Title 21: Food and Drugs
PART 1271—HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
Subpart B—Procedures for Registration and Listing
§ 1271.21 When do I register, submit an HCT/P list, and submit updates?
§ 1271.25 What information is required for establishment registration and HCT/P listing?
§ 1271.26 When must I amend my establishment registration?
§ 1271.27 Will FDA assign me a registration number?
§ 1271.37 Will establishment registrations and HCT/P listings be available for inspection, and how do I request information on registrations and listings?
