Systems Qualification

To help you navigate the highly regulated and complex pharmaceutical and biotechnology industries, we offer a wide range of qualification services to ensure that your system is fully operational for your specific process. 

We understand the need for quality, cost containment and regulatory compliance. With our functionality testing reports, we provide you the correct documentation to be used for system verification before moving to routine testing. We can also support you for your method validation.

For water systems in regulated labs, discover our Service Pharma™ Plans. Preventive maintenance programs are designed to enhance performance and extend lifetime in validated environments.

We understand the need for quality, cost containment, and regulatory compliance when it comes to the validation of your microbiology methods. With our validation protocols, we provide you the correct documentation to be used for audits and in front of the regulatory authorities. When on-site with a customer, our validation engineers ask the right questions as well as understand your application and the validation requirements of your equipment.