Russell Wilson

Client Lead/Sr. Compliance Consultant

He is dedicated to ensuring that your projects are completed with unparalleled customer service and quality. With over 15 years of experience in biopharmaceutical QA, my background spans the full breadth of GxP through every phase of drug development (preclinical to commercial). With principle expertise in GMP, Russell has worked on projects supporting the manufacturing of most types of therapies including drugs, biologics, sterile injectable/ophthalmic, cell and gene therapies, radioactive PET tracers, in vitro diagnostics, RNA therapeutics, devices, combination and OTC products. Holding a Ph.D. in Pharmaceutical Sciences and an MS in Quality Assurance and Regulatory Affairs, he can also support more specialized GxP projects according to the breadth of education and experience I have obtained through the years.  He looks forward to working with you on your projects and ensuring that QACV Consulting helps your products reach your patients in a safe and compliant manner.