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Medical Device Reprocessing Validation

Reprocessing Validation

Enabling the Reuse of Single-Use Medical Devices Safely and Efficiently

In an era where sustainability and cost-efficiency are paramount, the medical industry faces unprecedented challenges and opportunities such as regulatory changes and demand for product development. Wickham Micro Ltd, a partner laboratory of Cormica, is proud to introduce our advanced Medical Device Reprocessing services to evaluate the effectiveness of cleaning, disinfection and sterilisation. We specialise in conducting Reprocessing Validations that meet stringent regulatory requirements, ensuring the safe and effective reuse of single-use medical devices.

Why Choose Wickham Micro for Medical Device Reprocessing Validation?

Commitment to Excellence - At Wickham Micro, we uphold the highest standards of quality, reliability, and customer service. Our processes are certified to GMP, GLP and FDA affirming our commitment to precision and reliability.

Expertise in Diverse Testing Fields - Our extensive array of services throughout the Cormica group — Biocompatibility & Toxicology, Microbiology, Sterility & Environmental, Functional and Performance Testing, Chemical Analysis, Packaging, Seal & Transit Testing — allows us to offer a comprehensive approach to Medical Device Reprocessing.

Customised Solutions - Understanding that each client has their own unique needs, our expert team of scientists, engineers, and regulatory advisors tailor Reprocessing Validations to meet your specific criteria.


What is Reprocessing Validation?

Reprocessing Validation is a rigorous testing procedure that ensures the safe and effective reuse of single-use medical devices by confirming they meet all necessary quality and regulatory standards.

Why You Should Do Reprocessing Validation?

Implementing Reprocessing Validation is crucial for ensuring patient safety, complying with regulatory guidelines, and contributing to sustainable healthcare practices by enabling the reuse of single-use medical devices. It also provides evidence to support the cleaning, disinfection and sterilization techniques used for the device detailed in the Instructions for use (IFU).

How Does Reprocessing Validation Work?

Reprocessing Validation works by subjecting reprocessed medical devices to a series of specialized tests, such as sterility, cleaning validations and functional assessments, to verify that they meet stringent quality and safety benchmarks before re-entry into clinical use.


Our Services in Medical Device Reprocessing

Reprocessing Validations

Our Reprocessing Validations are designed to rigorously test and confirm that the reprocessed medical devices meet all required safety and effectiveness benchmarks, thereby ensuring compliance with global regulations.

Quality Control and Assurance

Wickham Micro's meticulous quality control protocols are integrated at each stage of the reprocessing cycle, from initial examination to final release.

Advisory and Consultation Services

Our team offers professional guidance to navigate the intricate regulatory landscape, aiding in faster market entry for your reprocessed medical devices.


Contact Us

Ready to explore how Wickham Micro can assist with your Medical Device Reprocessing needs? Contact us to discuss customized solutions designed to meet your objectives.


Wickham Micro, a partner laboratory of Cormica, is dedicated to enhancing patient lives by enabling the safe and rapid launch of medical devices across the world. Choose Wickham Micro for cutting-edge solutions in Medical Device Reprocessing.

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