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Regulations last checked for updates: May 23, 2025

Title 21 - Food and Drugs last revised: May 19, 2025
All TitlesTitle 21Chapter IPart 607Subpart B - Subpart B—Procedures for Domestic Blood Product Establishments
  • § 607.20 - Who must register and submit a blood product list.
  • § 607.21 - Times for establishment registration and blood product listing.
  • § 607.22 - How to register establishments and list blood products.
  • § 607.25 - Information required for establishment registration and blood product listing.
  • § 607.26 - Amendments to establishment registration.
  • § 607.30 - Updating blood product listing information.
  • § 607.31 - Additional blood product listing information.
  • § 607.35 - Blood product establishment registration number.
  • § 607.37 - Public disclosure of establishment registration and blood product listing information.
  • § 607.39 - Misbranding by reference to establishment registration, validation of registration, or to registration number.
authority: 21 U.S.C. 321,331,351,352,355,360,371,374,381,393; 42 U.S.C. 262,264,271
source: 40 FR 52788, Nov. 12, 1975, unless otherwise noted.
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