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HHS - 21 CFR PART 600

BIOLOGICAL PRODUCTS: GENERAL

active, Most Current
Organization: HHS
Publication Date: 1 April 2015
Status: active
Page Count: 20

Document History

21 CFR PART 600
April 1, 2023
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2022
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2021
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2020
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2019
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2018
BIOLOGICAL PRODUCTS: GENERAL
As used in this subchapter: (a) Act means the Public Health Service Act (58 Stat. 682), approved July 1, 1944. (b) Secretary means the Secretary of Health and Human Services and any other officer...
21 CFR PART 600
April 1, 2017
BIOLOGICAL PRODUCTS: GENERAL
General Provisions Mailing addresses. (a) Licensed biological products regulated by the Center for Biologics Evaluation and Research (CBER). Unless otherwise stated in paragraph (c) of this...
21 CFR PART 600
April 1, 2016
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2015
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
21 CFR PART 600
April 1, 2014
BIOLOGICAL PRODUCTS: GENERAL
A description is not available for this item.
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References

This document references:
19 CFR PART 12 - SPECIAL CLASSES OF MERCHANDISE
Published by FAA on April 1, 2014
A description is not available for this item.
This document references:
19 CFR PART 125 - CARTAGE AND LIGHTERAGE OF MERCHANDISE
Published by FAA on April 1, 2014
This part is concerned with cartage and lighterage of merchandise and the duties and liabilities of cartmen and lightermen, as well as those parties authorized in § 112.2(b) to engage in cartage....
This document is referenced by:
TIR48 - Quality Management System (QMS) Recommendations on the Application of the U.S. FDA’s CGMP Final Rule on Combination Products
Published by AAMI on January 1, 2015
Inclusions This Technical Information Report (TIR) provides recommendations on the application of CGMPs for drugs, devices, biologics, and human cells, tissues, and cellular and tissue based products...
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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