Process Specific - Extractables Testing l VR Analytical

About VR Analytical

In 2001, President and Founder Raymond Colton saw a unique need in the bio/pharmaceutical industry and started a company that specialized in extractables and leachables testing.

Since then, the company has built a body of expertise that goes beyond how to run the instrumentation. Knowledge of polymer chemistry and polymeric additives with an understanding of the bio/pharmaceutical manufacturing process allows us to develop customized test packages that bio/pharmaceutical end users and suppliers need to mitigate the potential risk of extractables and leachables reaching patients, and to help companies prepare for regulatory submission.

Today, this need is more important than ever as bio/pharmaceutical companies, medical device manufacturers, manufacturers of single-use technologies, manufacturers of final packaging/delivery systems, and regulatory agencies all recognize the importance of CFR Part 211.65, which requires detecting and identifying compounds that may present a risk to the safety and efficacy of drugs during the manufacturing, storage, and delivery processes.

As a contract research organization (CRO) that specializes in outsourced analytical testing, VR Analytical continues to invest in a cGMP environment, including fully outfitted laboratories, advanced instrumentation, and scientific expertise to create additional value for its customers.

VR Analytical's Values

Scientific Integrity: Trust and accountability are integral to our role as leaders in the scientific community.

Mastery: We nurture our skills in a results-oriented environment of trust, empowerment and involvement.

Service: We respect others and hold a sense of responsibility as we seek opportunities to add exceptional value in all of our interactions.

Dedication: We work hard together because our individual success is directly linked to the success of our company.