Federal (United States) · Regulations
Subpart C — Donor Eligibility
10 sections
10 sections
- 21 C.F.R. § 1271.45What requirements does this subpart contain?
- 21 C.F.R. § 1271.47What procedures must I establish and maintain?
- 21 C.F.R. § 1271.50How do I determine whether a donor is eligible?
- 21 C.F.R. § 1271.55What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?
- 21 C.F.R. § 1271.60What quarantine and other requirements apply before the donor-eligibility determination is complete?
- 21 C.F.R. § 1271.65How do I store an HCT/P from a donor determined to be ineligible, and what uses of the HCT/P are not prohibited?
- 21 C.F.R. § 1271.75How do I screen a donor?
- 21 C.F.R. § 1271.80What are the general requirements for donor testing?
- 21 C.F.R. § 1271.85What donor testing is required for different types of cells and tissues?
- 21 C.F.R. § 1271.90Are there other exceptions and what labeling requirements apply?