21 CFR § 607.21 Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

§ 607.21 Times for establishment registration and blood product listing.

Current through Sep 8, 2026 · Read all of Part 607

The owner or operator of an establishment entering into an operation defined in § 607.3(d) shall register such establishment within 5 days after the beginning of such operation and submit a list of every blood product in commercial distribution at the time. If the owner or operator of the establishment has not previously entered into such operation (defined in § 607.3(d) of this chapter) for which a license is required, registration shall follow within 5 days after the submission of a biologics license application in order to manufacture blood products. Owners or operators of all establishments so engaged must register annually between October 1 and December 31 and must update their blood product listing every June and December.

[40 FR 52788, Nov. 12, 1975, as amended at 64 FR 56453, Oct. 20, 1999; 81 FR 60222, Aug. 31, 2016]

← § 607.20 Who must register and submit a blood product list.§ 607.22 How to register establishments and list blood products. →