Customer Service:
Mon - Fri: 8:30 am - 6 pm EST

 Historical

ISO 10993-16:1997

Biological evaluation of medical devices -- Part 16: Toxicokinetic study design for degradation products and leachables

This part of ISO 10993 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.


Content Provider
International Organization for Standardization [iso]


Others Also Bought

Biological evaluation of medical devices -- Part 13: Identification and quantification of degradation products ...
Biological evaluation of medical devices -- Part 9: Framework for identification and quantification of potential ...
Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity
Document History
Revised By:
Included in Packages
This standard is not included in any packages.
Amendments & Corrections
We have no amendments or corrections for this standard.
ANSI Logo

As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

CUSTOMER SERVICE
NEW YORK OFFICE
ANSI HEADQUARTERS