Rely on SteriTech for Expert Validation and Commissioning Assistance in the UK & Ireland
At SteriTech, we understand the critical importance of having equipment that is fully validated, commissioned, and compliant with regulatory requirements.

That's why we offer a comprehensive suite of validation and commissioning services designed to ensure that your equipment meets the highest industry standards.
Customised Validation and Commissioning
Risk-Based Validation: We use risk-based validation strategies to ensure that your equipment is fully compliant and optimised for maximum efficiency, while minimising costs and reducing project timelines.

GMP Documentation: Complete GMP documentation services, including the development of URS, Design Specification documents, and GMP risk-based documentation to support the execution of CQV activities.

Installation and Commissioning Support: Hands-on support to help ensure that your equipment is installed correctly and in compliance with all applicable regulations.
Trust Us
Our expert team provides installation assistance, C&Q engineering, and comprehensive validation and compliance support to help you achieve operational excellence.

With SteriTech's help, you'll be prepared to meet the requirements of even the most stringent regulatory agencies, giving you peace of mind and confidence in your operations.
Enquire Today
Registered in Ireland as SteriTech Process Solutions Limited - Company number: 654374
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