GB/T 16886.16-2021 Active National standards

GB/T 16886.16-2021 Biological evaluation of medical devices—Part 16:Toxicokinetic study design for degradation products and leachables

GB/T 16886.16-2021 Biological evaluation of medical devices—Part 16:Toxicokinetic study design for degradation products and leachables

Publish Date: 2021-11-26 Implement Date: 2022-12-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us
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Basic Information

Standard Code: GB/T 16886.16-2021
Standard Type: National standards
Standard Status: Active
is_force_gb: no
CCS Name: Medical devices
ICS Name: Laboratory medicine
Publish Date: 2021-11-26
Implement Date: 2022-12-01
Pages: 17 pages

Scope

This document stipulates the principles of designing and conducting pharmacokinetic studies related to medical devices. Appendix A describes the issues to be considered in pharmacokinetic studies during the biological evaluation of medical devices. This document applies to pharmacokinetic studies of degradation products and leachables in medical devices.

Development Information

Word Count: 35 Thousand words Pages: 17 pages

Same series standard

Replace the following standards

Referenced Standards

ISO 10993-1

Adopt standards

ISO 10993-16:2017

Related Standards

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