Improving Product Quality During Technical Transfers

  • The definition of Technology Transfer and its many applications
  • Planning for tech transfer the “right way,” using “Calculated Risk Reduction” and other tools to ensure all bases are covered
  • Common pitfalls and best practices – what to do, and what not to do
  • Ways to ensure optimal planning and execution using actionable tools

Eric Good
Director, Compliance
ProPharma Group

Dr. Eric Good is an energetic leader with extensive U.S. and international manufacturing, project management, Consent Decree and quality systems experience with Fortune 500 Companies. Dr. Good has 29 years of award winning high-performance. He is an active leader in organizations with operational and compliance challenges. He has spoken both domestically and internationally about Quality Compliance and Technology Transfers. As a former Director of Project Management & Sustainable Compliance, Dr. Good was tasked with global technical transfer of products from Clinical to Commercial manufacturing. While each transfer averaged between 12-18 months, all was accomplished while under compliance remediation programs with global, cross-functional teams. Dr. Good has served as a technical transfer leader while working in Manufacturing and Quality leadership roles.

ProPharma Group is a global industry leader in comprehensive compliance services that span the entire lifecycle of pharmaceuticals, biologics, and medical devices. With more than 1,000 colleagues worldwide, ProPharma Group provides an unmatched variety of compliance related services including medical information, pharmacovigilance, clinical safety, regulatory affairs, and a continuously expanding range of compliance, quality assurance, validation, and consulting services. As an international, independent, single-source provider, ProPharma Group is here to support your needs.