Title 21

PART 1271 SUBPART C

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

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