Walk through the critical activities and success factors required for effective and efficient technology transfer, as well as requirements for planning, execution, and assimilation of technology and knowledge transfer. At the conclusion of this online course, participants will have knowledge of:
- Critical activities and success factors required for an effective and efficient technology transfer
- Requirements for planning, execution, and assimilation of technology and knowledge transfer
Attendance suggested for:
- Years in industry: 0-4 to 5-14
- Ideal audiences are those with 2+ years of industry experience that want to supplement their industry knowledge about a specific topic(s)
Charles F. Carney has nearly 40 years of experience in pharmaceutical drug product development, manufacturing, and analytical control. His industrial experience was gained at Wyeth (formerly Ayerst Laboratories) and Boehringer Ingelheim. For the last 15 years of his corporate service, he was the associate director of investigational supplies in the Connecticut R&D Center of Boehringer Ingelheim. Since 2003 he has been a consultant for Seraphim Life Sciences Consulting, LLC. His responsibilities have included performing and managing pharmaceutical, analytical, and GMP compliance aspects of drug product development, including the outsourcing, validation, and technology transfer aspects and the quality control, and facility design for commercial drug products. He is a member of ISPE, ACS, and AAAS. He has published and presented papers extensively in the areas of pre-formulation, formulation, and control of manufacturing operations for clinical drug products. He also has published and presented concepts in the areas of outsourcing of manufacturing and control, and for optimizing international operations. He is a co-editor of the second edition of “Drug Products for Clinical Trials” (Taylor & Francis, 2006).