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HHS - 21 CFR PART 606

CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS

active, Most Current
Organization: HHS
Publication Date: 1 April 2015
Status: active
Page Count: 14

Document History

21 CFR PART 606
April 1, 2023
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2022
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2021
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2020
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2019
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2018
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2017
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
Definitions. As used in this part: (a) Blood means a product that is a fluid containing dissolved and suspended elements which was collected from the vascular system of a human. (b) Unit means the...
21 CFR PART 606
April 1, 2016
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2015
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
21 CFR PART 606
April 1, 2014
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
A description is not available for this item.
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References

This document is referenced by:
CLSI GP47 - Management of Critical- and Significant-Risk Results
Published by CLSI on December 1, 2015
This guideline is intended for laboratory directors, managers, and personnel who develop and implement policies and processes for reporting laboratory results that need urgent clinical review. This...
This document is referenced by:
DI-TCSP-82040 - RESEARCH AND DEVELOPMENT OF MEDICAL PRODUCTS REGULATED BY THE U.S. FOOD AND DRUG ADMINISTRATION (FDA)
Published by NPFC on May 3, 2016
Use/relationship: This Data Item Description (DID) is published by the U.S Army Medical Research & Materiel Command (USAMRMC) to facilitate the acquisition of technical data to support the research...
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