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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 610 - PART 610—GENERAL BIOLOGICAL PRODUCTS STANDARDS
Subpart A [§ 610.1 - § 610.2] - Subpart A—Release Requirements
Subpart B [§ 610.9 - § 610.18] - Subpart B—General Provisions
Subpart C - Subparts C—D [Reserved]
Subpart E [§ 610.39 - § 610.48] - Subpart E—Testing Requirements for Relevant Transfusion-Transmitted Infections
Subpart F [§ 610.50 - § 610.53] - Subpart F—Dating Period Limitations
Subpart G [§ 610.60 - § 610.68] - Subpart G—Labeling Standards
authority:
21 U.S.C. 321
,
331
,
351
,
352
,
353
,
355
,
360
,
360
c,
360
d,
360
h,
360
i,
371
,
372
,
374
,
381
;
42 U.S.C. 216
,
262
,
263
,
263
a,
264
source:
38 FR 32056, Nov. 20, 1973, unless otherwise noted.
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