Beth Farinha, MS
Associate Principal Consultant
Beth Farinha provides Quality Assurance, Quality Management Systems, Compliance, and Regulatory Affairs support to the Sponsor of healthcare products. Her nearly 20 years of experience within industry includes interpretation of GxP regulations and ICH standards, as well as the establishment, implementation, and maintenance of regulatory compliant systems and procedures. Beth’s previous work experience includes pharmaceuticals, biologics, and medical devices with a strong emphasis on analytics for fortune 500 companies. She has held roles in CMC Quality Assurance, GxP auditing, Regulatory Affairs supporting oncology clinical trials, and Regulatory Affairs supporting Risk Evaluation Mitigation Strategy (REMS) FDA submissions. She has both led and been an active contributor for the development, implementation, and continuous improvement of quality systems from research through commercial activities. Beth has an M.S. in Health and Regulatory Affairs from Massachusetts College of Pharmacy and Health Sciences and a B.S. in Biochemistry, Bridgewater State University (formerly Bridgewater State College), Bridgewater, Massachusetts.