Validation of software is not a choice for customers in the life science, pharmaceutical and medical device industries. It is a requirement set by agencies around theworld. For many regulated companies today, validation has become a costly and time-consuming aspect of installing or upgrading Quality Management Software(QMS). But validation does not need to be a burden that prevents companies from investing in software that can improve product quality, safety and efficiency.
ETQ’s validation offerings for life science companies are fully aligned with regulations and industry guidance and offer a comprehensive approach based on guidance like GAMP 5.