Albert Rego, Ph.D. wpGI-Logic
Albert Rego, Ph.D.
Albert Rego, Ph.D., M.B.A., is a scientific consultant to the regulated industries, with over 30 years of experience in the pharmaceutical and medical device industries. His areas of specialization are in the national and international regulatory aspects of the scientific testing requirements for chemical, biological and sterilization technologies. Albert Rego’s experience is focused on performing, directing, designing, and evaluating clinical and non-clinical studies for pharmaceuticals and medical devices. Selective expertise includes chemical stability testing, medical device evaluations, statistical design and interpretation, regulatory submissions, chemical hygiene plans, analytical chemistry methodologies, and sterilization validation.
Selective expertise includes the coordination and direction of defining Specified Regulatory and Quality System related requirements, Strategic considerations, and Tactical considerations for start up operations in the area of medical products, including medical devices and pharmaceuticals. Well over fifty (50) startup operations have gained benefit from Rego engaging this expertise and service.