White Paper

Automated Validation

Software validation is one of the top challenges for highly regulated Medical Device manufacturers who are tasked with speeding products from R&D to market, while also ensuring process compliance, reliability and product quality.

Validation is expensive, resource intensive and time consuming and the effort required to upgrade and revalidate processes often prevents companies from unlocking the full value of their production software. In this new white paper, learn how next generation Automated Validation from Critical Manufacturing can reduce the validation of MES implementations from month to days.

Fill out the form to read the White Paper