Edwin R. Thompson:
Ed is the founder and President of Pharmaceutical Manufacturing Research Services, Inc. He has over 40 years' experience in pharmaceutical sales, marketing, product development, research and development, and manufacturing.
Jonathan M. Neafsey:
Director, Manufacturing Services
Jon holds a Master’s Degree in Biomedical Engineering and has over 5 years’ experience in pharmaceutical product development, clinical manufacturing, and commercial production. He has played key roles in GMP compliance in drug development efforts from discovery through phase IV clinical trials and commercial production.
Matthew E. Anderson:
Director, Analytical Services
Matt has over 15 years' experience in pharmaceutical analytical services, quality control, and research and development. His experience includes raw materials, intermediates, and finished products in a variety of dosage forms. Matt has extensive experience in the area of drug product and drug substance stability. He joined PMRS in 2000, and is responsible for all analytical service operations including method development, validation and transfer, quality control functions, and laboratory compliance to customer, SOP, and GMP requirements. Matt was responsible for the design, infrastructure, and implementation of the new 11,000 sq ft analytical laboratory, the PMRS Laboratory Information Management System (LIMS), and the innovative new Electronic Notebook system utilized by PMRS.
Drew A. Kirby:
Director, Quality Management & Technology
Drew Kirby has over 15 years' healthcare and pharmaceutical experience in regulatory compliance, information systems and security, along with project and vendor management.
His background includes regulatory and client audits, systems and process validation with a focus on technology development. He joined PMRS in 2006, and is responsible for the quality management systems and the technology direction of the company.