We provide comprehensive equipment validation services, including full documentation package development, execution of validation activities, and seamless integration into production environments. Our approach is tailored to meet your specific business needs and operational processes, all while maintaining strict compliance with current regulatory guidelines and industry best practices
Compliance is at the core of everything we do. We ensure all activities are aligned with the lastest regulatory requirements and industry standards, including EU GMP, FDA, USP, and GAMP guidelines. Our team is dedicated to maintaining a robust quality framework, promoting data integrity, and delivering validation solutions that stand up to regulatory scrutiny. Giving you confidence in both your processes and outcomes
While we support all aspects of pharmaceutical equipment validation, our core expertise lies in visual inspection - particularly automated visual inspection (AVI) systems. We specialise in process mapping, system optimisation, and integrating AVI solutions that align with both regulatory expectations and operational efficiency. From manual inspection through to fully automated lines, we bring deep understanding and hands-on experience to ensure reliable and compliant inspection performance
Mon | 09:00 – 17:00 | |
Tue | 09:00 – 17:00 | |
Wed | 09:00 – 17:00 | |
Thu | 09:00 – 17:00 | |
Fri | 09:00 – 17:00 | |
Sat | Closed | |
Sun | Closed |
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