SciLucent’s staff includes scientific, medical, and regulatory professionals with expertise and experience in all aspects of healthcare product development and marketed product support.
Thomas L. McMahon
Chemistry, Manufacturing, and Controls Development and Implementation; Outsourcing Management; Quality Systems and Compliance; Regulatory Strategy, Documentation, and Implementation
Tom McMahon specializes in drug development process management; chemistry, manufacturing, and controls program administration and submission preparation; due diligence evaluations in support of potential partnering and in-licensing opportunities; proactive and remedial cGMP compliance activities; quality systems management; and scientific/regulatory issue research and analysis. He has aided numerous pharmaceutical and biopharmaceutical clients with product development, project management, corporate and facility compliance reviews, critical reviews of scientific issues, regulatory strategic planning and submission compilation, and in establishing and optimizing quality systems. Tom's expertise includes monoclonal antibodies, therapeutic proteins, oncology drugs, and cardiovascular drugs.
