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HHS - 21 CFR PART 250

SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS

active, Most Current
Organization: HHS
Publication Date: 1 April 2018
Status: active
Page Count: 9

Document History

21 CFR PART 250
April 1, 2022
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2021
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2019
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2018
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2017
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2016
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2015
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
21 CFR PART 250
April 1, 2014
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
A description is not available for this item.
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References

This document is referenced by:
DODD 5101.15 - DoD Medical Materiel Executive Agent (MMEA) Implementation Guidance
Published by DOD on August 31, 2018
PURPOSE. In accordance with the authority in DoD Directive (DoDD) 5134.01 (Reference (a)), this Instruction: a. Implements the policy in DoDD 5101.09E (Reference (b)) by assigning responsibilities...
This document is referenced by:
AFI 44-105 - THE AIR FORCE BLOOD PROGRAM
Published by AIR FORCE on January 10, 2019
A description is not available for this item.
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