COURSE DESCRIPTION
You will gain a fundamental comprehension of technology transfer in the pharmaceutical industry, including the transfer of analytical methods, quality control standards, packaging components/operations, and various dosage forms from R&D to manufacturing. The course provides an overview of scale-up and technology transfer of solid dosage forms, injectables, and semisolids. This 8-hour accredited course will delve into the challenges of transfers within and outside a company, including transfers to/from international sites and third parties. Best practices to avoid common pharmaceutical technology transfer issues will be discussed. The course will address issues affecting changes to batch size, formulation, packaging components, site of manufacture, manufacturing process, analytical methods, specifications, and processing equipment changes, with practical examples from experienced speakers. The importance of technology transfer teams and the roles and responsibilities of project managers and team members will be emphasized. Additionally, participants will engage in interactive case studies, based on real-world examples, to develop collaborative strategies and plans to execute complex transfers with short timelines. The course is designed for professionals involved in the technology transfer of prescription (innovator and generic) and over-the-counter drug products.
COURSE INSTRUCTOR
Take a look at our instructor scheduled for this course.

Walter Chambliss
Professor Emeritus of Pharmaceutics and Drug Delivery
University of Mississippi

Mukund “Mike” Yelvigi
Principal and Managing Partner
Center for Pharmaceutical Integration, LLC
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