The Cleaning Validation Revolution Is Here — And Compliance Associates Is Leading It
Mississauga, Canada – March 25, 2026 / Validator /
Compliance Associates has launched Cleaning Validation for Validator — a purpose-built module that automates the entire cleaning validation lifecycle, end to end. Two clients, already deep in the Validator ecosystem, signed on before the official launch. They didn’t need convincing. They’d seen what Validator does for the rest of their validation program and knew this would be no different.
That’s exactly the kind of confidence Compliance Associates is built on — and exactly why now is the right time to bring Cleaning Validation to market.
Built From the Ground Up. Not Bolted On.
Cleaning validation is one of the highest-risk areas in any regulatory audit. A missed swab test, an outdated SOP, fragmented documentation — and suddenly a team is scrambling. Some platforms claim to handle cleaning validation. Validator actually does it.
Where others offer documentation workflows dressed up as automation, Validator’s Cleaning Validation module automates every meaningful activity in the process: MACO calculations, risk-based revalidation recommendations using built-in FMEA models, digital cleaning logs, worst-case and hold time study management, CQA tracking with configurable sampling plans, and real-time statistical analysis of cleaning test data — all with complete audit trails, electronic signatures, and full integration into existing ERP, LIMS, and LMS systems.
This is what purpose-built looks like. Not a checklist in a document editor. Not a form that lives in a folder. A true automation platform that runs the process.
Validator follows the GAMP 5 V-Model across all four stages — Planning, Design, Testing, and Reporting — so every protocol, result, and approval is digitized, traceable, and mapped back to requirements. When changes happen, built-in change control and periodic review tools keep teams compliant without the scramble.
“Our clients didn’t wait for the launch announcement — they signed on because they’d already seen what Validator can do,” said Victor Zurita, CEO of Compliance Associates. “Cleaning validation has always been one of the most documentation-intensive, audit-exposed areas in the industry. We built a module that actually automates it — not just digitizes it. There’s a real difference, and the industry is going to feel it.”
A Competitive Gap — And a Clear Leader
Compliance Associates has been automating validation for regulated industries since 2003. Validator already delivers over 40% efficiency gains across Computer System Validation, Process Validation, and Equipment Qualification — with a 100% implementation success rate across more than 300 clients and 20,000 active users worldwide. Cleaning Validation brings the same depth of automation to an area the industry has long managed the hard way.
Full implementation and configuration is typically complete within three months. The module is built for pharmaceutical, biotechnology, medical device, and life sciences organizations operating under FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and ISO standards.
About Compliance Associates
Compliance Associates has been a trusted partner to the life sciences industry since 2003 — not just as a software provider, but as practitioners who have lived and breathed validation from the inside. Validator is the direct result of that experience: an automation platform built by people who know what auditors look for, what teams struggle with, and what it actually takes to stay compliant at scale.
To book a demo or learn more, visit www.validatorvlms.com or contact info@complianceassociates.ca.
Contact Information:
Validator
Suite 31, 5160 Explorer Drive
Mississauga, ON L4W 4T7
Canada
Victor Zurita
866-961-7275
https://www.validatorvlms.com
