21 CFR Part 610 - PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS

  1. Subpart A—Release Requirements (§§ 610.1 - 610.2)
  2. Subpart B—General Provisions (§§ 610.9 - 610.18)
  3. Subparts C—D [Reserved]
  4. Subpart E—Testing Requirements for Relevant Transfusion-Transmitted Infections (§§ 610.39 - 610.48)
  5. Subpart F—Dating Period Limitations (§§ 610.50 - 610.53)
  6. Subpart G—Labeling Standards (§§ 610.60 - 610.68)
Authority:
21 U.S.C. 321, 331, 351, 352, 353, 355, 360, 360c, 360d, 360h, 360i, 371, 372, 374, 381; 42 U.S.C. 216, 262, 263, 263a, 264.
Source:
38 FR 32056, Nov. 20, 1973, unless otherwise noted.
Cross References:

For U.S. Customs Service regulations relating to viruses, serums, and toxins, see 19 CFR 12.21–12.23. For U.S. Postal Service regulations relating to the admissibility to the United States mails see parts 124 and 125 of the Domestic Mail Manual, that is incorporated by reference in 39 CFR part 111.

The following state regulations pages link to this page.


Washington