§1271.25. What information is required for establishment registration and HCT/P listing? — Inbound Citations
21 C.F.R. § 1271.25
Statutory Authority
Cited by 3 regulations in release Current.
Citations to 21 C.F.R. § 1271.25 as a whole
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(a) You must use the electronic registration and listing system at http://www.fda.gov/cber/tissue/tisreg.htm in accordance with § 1271.25 for:(1) Establishment registration,(2) HCT/P listings, and
Citations to §1271.25(b)
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(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.
Citations to §1271.25(c)
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(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.