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Code · CFR · Title 21 — Food and Drugs · Part 607 — Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices · § 607.21

§ 607.21. Times for establishment registration and blood product listing.

139 words·~1 min read·/us/cfr/t21/s§ 607.21·

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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]
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§ 607.21
Times for establishment registration and blood product listing.
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