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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER L—REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION
  6. PART 1271—HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
  7. Subpart C—Donor Eligibility

21 CFR Part 1271 - Subpart C - Donor Eligibility

  • CFR
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  1. § 1271.45 What requirements does this subpart contain?
  2. § 1271.47 What procedures must I establish and maintain?
  3. § 1271.50 How do I determine whether a donor is eligible?
  4. § 1271.55 What records must accompany an HCT/P after the donor-eligibility determination is complete; and what records must I retain?
  5. § 1271.60 What quarantine and other requirements apply before the donor-eligibility determination is complete?
  6. § 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?
  7. § 1271.75 How do I screen a donor?
  8. § 1271.80 What are the general requirements for donor testing?
  9. § 1271.85 What donor testing is required for different types of cells and tissues?
  10. § 1271.90 Are there other exceptions and what labeling requirements apply?
Source:
69 FR 29830, May 25, 2004, unless otherwise noted.

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