Title 21

PART 1271 SUBPART C

Subpart C - Donor Eligibility Source:69 FR 29830, May 25, 2004, unless otherwise noted.

• 42 U.S.C. 216, 243, 263a, 264, 271.
• Source: 66 FR 5466, Jan. 19, 2001, unless otherwise noted.

21:8.0.1.5.60.3.1.1	SECTION 1271.45	1271.45 What requirements does this subpart contain
21:8.0.1.5.60.3.1.2	SECTION 1271.47	1271.47 What procedures must I establish and maintain
21:8.0.1.5.60.3.1.3	SECTION 1271.50	1271.50 How do I determine whether a donor is eligible
21:8.0.1.5.60.3.1.4	SECTION 1271.55	1271.55 What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain
21:8.0.1.5.60.3.1.5	SECTION 1271.60	1271.60 What quarantine and other requirements apply before the donor-eligibility determination is complete
21:8.0.1.5.60.3.1.6	SECTION 1271.65	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
21:8.0.1.5.60.3.1.7	SECTION 1271.75	1271.75 How do I screen a donor
21:8.0.1.5.60.3.1.8	SECTION 1271.80	1271.80 What are the general requirements for donor testing
21:8.0.1.5.60.3.1.9	SECTION 1271.85	1271.85 What donor testing is required for different types of cells and tissues
21:8.0.1.5.60.3.1.10	SECTION 1271.90	1271.90 Are there other exceptions and what labeling requirements apply

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