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Code · CFR · Title 21 — Food and Drugs · Part 606 — Current Good Manufacturing Practice for Blood and Blood Components · § 606.40

§ 606.40. Facilities.

287 words·~1 min read·/us/cfr/t21/s§ 606.40·

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

Facilities shall be maintained in a clean and orderly manner, and shall be of suitable size, construction and location to facilitate adequate cleaning, maintenance and proper operations. The facilities shall:
(a)Provide adequate space for the following when applicable:
(1)Private and accurate examinations of individuals to determine their eligibility as blood donors.
(2)The withdrawal of blood from donors with minimal risk of contamination, or exposure to activities and equipment unrelated to blood collection.
(3)The storage of blood or blood components pending completion of tests.
(4)The quarantine storage of blood or blood components in a designated location pending repetition of those tests that initially gave questionable serological results.
(5)The storage of finished products prior to distribution.
(6)The quarantine storage, handling and disposition of products and reagents not suitable for use.
(7)The orderly collection, processing, compatibility testing, storage and distribution of blood and blood components to prevent contamination.
(8)The adequate and proper performance of all steps in plasmapheresis, plateletpheresis and leukapheresis procedures.
(9)The orderly conduction of all packaging, labeling and other finishing operations.
(b)Provide adequate lighting, ventilation and screening of open windows and doors.
(c)Provide adequate, clean, and convenient handwashing facilities for personnel, and adequate, clean, and convenient toilet facilities for donors and personnel. Drains shall be of adequate size and, where connected directly to a sewer, shall be equipped with traps to prevent back-siphonage.
(d)Provide for safe and sanitary disposal for the following:
(1)Trash and items used during the collection, processing and compatibility testing of blood and blood components.
(2)Blood and blood components not suitable for use or distribution. [40 FR 53532, Nov. 18, 1975, as amended at 80 FR 29895, May 22, 2015]
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