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Electronic Code of Federal Regulations (e-CFR)
Title 21 - Food and Drugs
CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER F - BIOLOGICS
PART 600 - BIOLOGICAL PRODUCTS: GENERAL
Subpart D - Reporting of Adverse Experiences

21 CFR Subpart D - Reporting of Adverse Experiences

CFR

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§ 600.80 Postmarketing reporting of adverse experiences.
§ 600.81 Distribution reports.
§ 600.82 Notification of a permanent discontinuance or an interruption in manufacturing.
§ 600.90 Waivers.

Source:

59 FR 54042, Oct. 27, 1994, unless otherwise noted.

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