21 CFR Part 606 · Current Good Manufacturing Practice for Blood and Blood Components

§ 606.20 Personnel

Subpart B - Organization and Personnel Official text on eCFR Amendment history

(a) [Reserved]

(b) The personnel responsible for the collection, processing, compatibility testing, storage or distribution of blood or blood components shall be adequate in number, educational background, training and experience, including professional training as necessary, or combination thereof, to assure competent performance of their assigned functions, and to ensure that the final product has the safety, purity, potency, identity and effectiveness it purports or is represented to possess. All personnel shall have capabilities commensurate with their assigned functions, a thorough understanding of the procedures or control operations they perform, the necessary training or experience, and adequate information concerning the application of pertinent provisions of this part to their respective functions.

(c) Persons whose presence can adversely affect the safety and purity of the products shall be excluded from areas where the collection, processing, compatibility testing, storage or distribution of blood or blood components is conducted.

Independent copy, not an official legal edition. 21 CFR is a U.S. Government work in the public domain; this text comes from the eCFR and the annual CFR edition, and may lag recent amendments. The authoritative version is on ecfr.gov. Compliome is not affiliated with or endorsed by FDA. Not legal advice.

What FDA inspectors cite under § 606.20

Form FDA 483 observations citing this section, fiscal years 2009–2025 (Biologics).

  • Qualifications of responsible personnel 97
  • Exclusion of certain persons 2

Warning letters citing § 606.20

1 FDA warning letters since 2017 cite this section :

FDA guidance that cites § 606.20

Amendment history

Federal Register documents that created or amended this section.