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Eurotherm can offer assistance with validation activities throughout your project lifecycle.

Many of our pharmaceutical, biotechnology and medical devices customers request work to the GAMP Guide for Validation of Automated Systems – guidelines which have become de facto standard for Good Automated Manufacturing Practice in the healthcare industries.

We have a long history of projects successfully validated to ISPE GAMP5 guidelines including many which are now operating in FDA regulated environments.

Our in house experts develop a large amount of Qualification/Validation Template Documentation to save time and cost on Engineering and to deliver peace of mind during the Validation/Audit on site

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