
ISO 10993:2017
ISO 10993:2017 Biological evaluation of medical devices – Part 16: Toxicokinetic study design for degradation products and leachables
CDN $186.00
SKU: 7c60b3b451b2
Categories: ICS:11.100.20, SUSTAINABLE_DEVELOPMENT_GOAL:3
Description
ISO 10993-16:2017 provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.
Edition
3
Published Date
2017-05-16
Status
PUBLISHED
Pages
13
Format 
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment
Abstract
ISO 10993-16:2017 provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-

ISO 17117:2022 Health informatics – Terminological resources – Part 2: Implementation Capability (TIC)
CDN $124.00 Add to cart -

ISO 16972:2020 Respiratory protective devices – Vocabulary and graphical symbols
CDN $82.00 Add to cart -

ISO 9687:2015 Dentistry – Graphical symbols for dental equipment
CDN $295.00 Add to cart -

ISO 17097:2024 3-D human body scan data – Methods for the processing of human body scan data
CDN $186.00 Add to cart







