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HHS - 21 CFR PART 520

ORAL DOSAGE FORM NEW ANIMAL DRUGS

active
Organization: HHS
Publication Date: 1 April 2022
Status: active
Page Count: 115

Document History

21 CFR PART 520
April 1, 2023
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2022
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2021
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2020
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2019
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2018
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2017
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2016
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2015
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
21 CFR PART 520
April 1, 2014
ORAL DOSAGE FORM NEW ANIMAL DRUGS
A description is not available for this item.
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References

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....
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