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 320

BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS

active, Most Current
Organization: HHS
Publication Date: 1 April 2021
Status: active
Page Count: 16

Document History

21 CFR PART 320
April 1, 2023
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2021
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2020
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2019
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2018
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
Definitions. The definitions contained in § 314.3 of this chapter apply to those terms when used in this part.
21 CFR PART 320
April 1, 2017
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
Definitions. The definitions contained in § 314.3 of this chapter apply to those terms when used in this part.
21 CFR PART 320
April 1, 2016
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2015
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
21 CFR PART 320
April 1, 2014
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
A description is not available for this item.
View Less
View All

References

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