Verification and Validation of Sterilization Methods for Instruments/Equipment Used in Survival Surgery
IACUC Policy: 050-03, Effective Date: 10/18/2013, Last Revision: 04/18/2025
Overview/Purpose
Verification and validation of sterilization methods are necessary to ensure materials have been properly sterilized. The purpose of this policy is to ensure verification and validation of the process used for sterilization of survival surgery equipment and instruments.
Definitions
- Verification: verification of sterilizer function includes the use of chemical control indicators (e.g. chemical indicator tape or indicator test strips) to ensure the appropriate conditions have been reached during the cycle. Chemical control indicators are specific to the sterilization method being used and care must be taken to select the appropriate indicator. Though chemical control indicators are useful to ensure adequate temperatures or gas exposures have been reached during the cycle, they cannot verify the length of time that the parameters were maintained and therefore validation is still required.
- Validation: validation of sterilization uses a biological control (e.g. Verify®, 3M™ Attest™) to confirm lack of microbial growth. Biological controls use heat-resistant microorganisms to determine the effectiveness of steam or chemical sterilization. Biological controls are sensitive and accurate and require a period of incubation to validate the effectiveness of the cycle. Similar to the chemical indicators, specific biological indicators are available for each sterilization method. Validation is not required when cold sterilants are used according to manufacturer's instructions.
Requirements
- A chemical control indicator must be used for verification of all items being sterilized for survival surgeries. Chemical control indicators provide instant notification of failures to reach the required cycle parameters.
- A chemical control indicator must be present on the outside package of all items being sterilized. Most surgical peel pouches have a built-in chemical control indicator.
- An additional chemical control indicator must be present on the inside of surgical packs prior to sterilizing to ensure adequate steam / gas penetration.
- The sterilization date must be present on the outside package or pouch.
- Unused items must be resterilized within 1 year from the date of initial sterilization, or if the outer covering is compromised.
- If chemical control indicators fail or if sterilization cycle does not complete, items must be resterilized prior to use.
- Autoclave or gas sterilizer validation must be performed semiannually.
- Documentation of semiannual validation must be available for review.
Additional Information/Guidance
Revision History
- 050-00 - new policy approved 10/18/2013
- 050-01 - revised to clarify verification and validation, the requirement for initials to be included on the outside package of autoclaved items was removed, unused autoclaved items must be resterilized within one year; approved 11/18/2016
- 050-02 - revised to clarify the definition for verification and include in the overview section that time and temperature depends upon the material sterilized; approved 11/15/2019
- 050-03 - policy reviewed and approved 11/18/2022
- 050-04 - review, updated guidance, and approved 04/18/2025
Article ID: 47
Created: May 21, 2024
Last Updated: May 21, 2025
Online URL: https://ohiostateresearch.knowledgebase.co/article/verification-and-validation-of-sterilization-methods-for-instruments-equipment-used-in-survival-surgery-47.html