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HHS - 21 CFR PART 329

NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT

active, Most Current
Organization: HHS
Publication Date: 1 April 2021
Status: active
Page Count: 2

Document History

21 CFR PART 329
April 1, 2023
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2021
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2020
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2019
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2018
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2017
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2016
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
21 CFR PART 329
April 1, 2015
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
A description is not available for this item.
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References

This document is referenced by:
CGA F-2 - GUIDELINE FOR FOOD GASES PRODUCT HAZARD ANALYSIS AND RISK-BASED PREVENTIVE CONTROL (HARPC) PROGRAM
Published by CGA/GAS on January 1, 2017
A description is not available for this item.
This document is referenced by:
C-4-OSHA - METHOD OF MARKING PORTABLE COMPRESSED GAS CONTAINERS TO IDENTIFY THE MATERIAL CONTAINED
Published by CGA on January 1, 1954
This is the 2nd edition, as cited, when purchased you will also receive the current edition of C-7, which has superseded C-4. Requirements for marking portable compressed gas containers, not...
This document is referenced by:
CGA PS-50 - FOOD GASES AND GENETICALLY MODIFIED ORGANISMS (GMO)
Published by CGA/GAS on January 1, 2019
A description is not available for this item.
This document is referenced by:
CGA P-2 - GUIDELINE FOR CHARACTERISTICS AND SAFE HANDLING OF MEDICAL GASES
Published by CGA/GAS on January 1, 2019
This publication describes the properties of common medical gases, medical gas containers, and safe practices and handling of these gases. This publication does not address the following: •...
This document is referenced by:
AAMI 60601-1-2 - MEDICAL ELECTRICAL EQUIPMENT – Part 1-2: General requirements for basic safety and essential performance – Collateral Standard: Electromagnetic disturbances – Requirements and tests
Published by AAMI on January 1, 2014
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document is referenced by:
CGA M-21 - GUIDELINE FOR DETERMINING PHARMACOVIGILANCE REPORTING REQUIREMENTS IN NORTH AMERICA (FOR THE U.S. & REFERENCE FOR CANADA)
Published by CGA/GAS on January 1, 2017
A description is not available for this item.
This document is referenced by:
C22.2 NO. 60601-1-2:16 - Medical electrical equipment — Part 1-2: General requirements for basic safety and essential performance — Collateral Standard: Electromagnetic disturbances — Requirements and tests
Published by CSA on January 1, 2016
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
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