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Regulations last checked for updates: Nov 22, 2024
Title 21 - Food and Drugs last revised: Nov 19, 2024
All Titles
Title 21
Chapter I
Part 1271
Subpart C - Subpart C—Donor Eligibility
§ 1271.45 - What requirements does this subpart contain?
§ 1271.47 - What procedures must I establish and maintain?
§ 1271.50 - How do I determine whether a donor is eligible?
§ 1271.55 - What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?
§ 1271.60 - What quarantine and other requirements apply before the donor-eligibility determination is complete?
§ 1271.65 - How do I store an HCT/P from a donor determined to be ineligible, and what uses of the HCT/P are not prohibited?
§ 1271.75 - How do I screen a donor?
§ 1271.80 - What are the general requirements for donor testing?
§ 1271.85 - What donor testing is required for different types of cells and tissues?
§ 1271.90 - Are there other exceptions and what labeling requirements apply?
authority:
42 U.S.C. 216
,
243
,
263a
,
264
,
271
source:
66 FR 5466, Jan. 19, 2001, unless otherwise noted.
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