Validation and Qualification of Manufacturing Automation Systems in the Life Sciences

Life sciences manufacturing, more than just about any other industry, is especially challenging due to the level of validation and qualification regulations surrounding every aspect of quality manufacturing solutions. The validation and qualification services landscape has changed many times in the 30 years Allurént Corporation has been in business offering automation engineering services to life sciences manufacturing clients worldwide.

Our most recent example is the implementation of E-2500 Risk-Based Validation by the life sciences industry that aims to simplify the validation and qualification process. In order to effectively guide our clients through this new process, Allurént has taken the lead in providing validation and qualification services specific to each industry we serve.

Over the years, we’ve dedicated our expert engineering team to adapt to new validation and qualification requirements to consistently help our customers navigate the latest automation engineering trends and manufacturing software developments while avoiding unexpected pitfalls.

Interested in finding out the most recent validation and qualification requirements affecting your company and the entire life sciences manufacturing industry? Contact Allurént Corporation for a no-obligation assessment of how our services and solutions will advance your manufacturing system today.