- ASTM E1766, 2015 Edition, Standard Test Method for Determination of Effectiveness of Sterilization Processes for Reusable Medical Devices
- ASTM E1891, 2010a Edition Reapproved in 2015, Standard Guide for Determination of a Survival Curve for Antimicrobial Agents Against Selected Microorganisms and Calculation of a D-Value and Concentration Coefficient
- ASTM E2752, 2010 Edition Reapproved in 2015, Standard Guide for Evaluation of Residual Effectiveness of Antibacterial Personal Cleansing Products
- BS EN 13727, 2012 Edition with Amendment A2, Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity in the medical area. Test method and requirements (phase 2, step 1)
- BS EN 14476, 2013 Edition with Amendment A1, Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity in the medical area. Test method and requirements (Phase 2/Step 1)
- DIN EN 556-2, 2015 Edition, Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 2: Requirements for aseptically processed medical devices (English Language Edition)
- DIN EN 14885, 2015 Edition, Chemical disinfectants and antiseptics - Application of European Standards for chemical disinfectants and antiseptics (English Language Edition)
- DIN EN ISO 11137-1, 2015 Edition, Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (English Language Edition)
For more standards like these, please see our Document Center List of Standards on Sterilization and Disinfection for the Healthcare Industry. A number of links will direct you to the various sub-sets for this classification.
You're also welcome to take a look at my previous post:
