UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

HHS - 21 CFR PART 556

TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD

active, Most Current
Organization: HHS
Publication Date: 1 April 2019
Status: active
Page Count: 15

Document History

21 CFR PART 556
April 1, 2019
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
A description is not available for this item.
21 CFR PART 556
April 1, 2018
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
General considerations; tolerances for residues of new animal drugs in food. (a) Tolerances established in this part are based upon residues of drugs in edible products of food-producing animals...
21 CFR PART 556
April 1, 2016
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
General considerations; tolerances for residues of new animal drugs in food. (a) Tolerances established in this part are based upon residues of drugs in edible products of food-producing animals...
21 CFR PART 556
April 1, 2015
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
A description is not available for this item.
21 CFR PART 556
April 1, 2014
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
General Provisions General considerations; tolerances for residues of new animal drugs in food. (a) Tolerances established in this part are based upon residues of drugs in edible products of...

References

This document is referenced by:
IEC 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 IEC on September 1, 2020
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:
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....
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....
Advertisement