Who We Are

CQV LLC (“CQV”) has become a recognized leader in providing a variety of compliance services to the Life Sciences Industry. As a full-service company we offer consulting services and project resources within the Quality Assurance, Laboratory, Clinical, IT/IM, Business Processes, Manufacturing, Operations and R&D settings.

A privately held, career based company established in 1994, CQV, along with our Global Alliance partners, provides services worldwide and has successfully executed projects throughout the US, Canada, Puerto Rico, Switzerland, France, Ireland, the UK, Spain, Mexico, China and Japan.

With a depth of expertise in all facets of the system life cycle we are able to assist our clients within any phase to reach their goal of running a lean but efficient operation. Our experienced staff can help with Requirements Definition, Vendor Selection, Configuration, Implementation, Testing & Validation, and Maintenance. Our ability to understand the FDA compliance issues associated with systems implementation underscores the value-add that we provide while supporting the systems integration and turnover to production. We typically provide systems integration and validation support within the Research & Development, Clinical Trials, Quality Assurance, Laboratory, IT/IM, Operations, Manufacturing and Distribution environments. CQV can evaluate and access your current business operations and provide low cost solutions to streamline processes and reduce regulatory exposure. The application and implementation of recommended standard solutions will increase harmonization and management of critical cross-functional business systems. Thus mitigating the risk of non-compliance, reducing costs, increasing profitability, and helping to achieve operational excellence.

Visit our Services section to find out the many areas where we have demonstrated expertise in the industry.