Rosanna M Goodrich approaches her audits with a keen eye for procedural conformity and risk management. She places great importance on staff training, control over received products, and effective process validations. Her reports often emphasize on thoroughness of CAPA and the importance of consistent documentation and equipment maintenance.

Rosanna M Goodrich is a meticulous FDA investigator with a keen interest in procedural efficiency, risk management, and validation of processes. She has demonstrated consistent emphasis on the criticality of compliance with established procedures, especially those concerning Corrective and Preventive Actions (CAPA), risk analysis, control over received products, and environmental conditions. Control of nonconforming products and adequate training for staff are other areas she deeply cares about. Rosanna's observations clearly indicate her inclination towards ensuring effective control over validated processes and maintaining routine equipment calibration.