Sterilization of Health Care Products - Radiation - Part 1: Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices (Adopted ISO 11137-1:2006, First Edition, 2006-04-15)

Publisher:
Canadian Standards Association / National Standard of Canada

Document status:

Active

Format:

Electronic (PDF)

Delivery time:

10 minutes

Delivery time (for Russian version):

200 business days

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This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO 11137 is limited to medical devices, it specifies requirements and provides guidance that may be applicable to other products and equipment.

Edition :	1st
File Size :	1 file , 930 KB
ISBN(s) :	1554364493
Note :	This product is unavailable in Russia, Ukraine, Belarus
Number of Pages :	56
Product Code(s) :	2418370, 2418371, 2418370
Published :	03/01/2007

CAN/CSA Z11137-1-07 (R2021) PDF

Sterilization of Health Care Products - Radiation - Part 1: Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices (Adopted ISO 11137-1:2006, First Edition, 2006-04-15)

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