Implementation of a Successful Technology Transfer Process

  • Product Id : FDB2301
  • Category : , ,
  • Presenter :
  • Scheduled On : July 26 2017 1:00 pm
  • Duration : 60 Minutes

This training will introduce the concepts associated with implementing a carefully defined technical and business governance programs along with clearly defined R&D to site transfer steps for successful implementation. It will cover the concepts associated with transferring the scientific technology needed to manufacture the product, processes to ensure the receiving manufacturing facility is ready for the product and tools and templates to help capture the knowledge.

At the end of the session, you should be able to:

  • Define technology transfer
  • Identify elements of the business process framework for managing technology transfers
  • Identify New Product transfer process
  • Explain benefits of technology transfer
  • Determine elements of a successful technology transfer

Why You Should Attend:

Successful transfer of pharmaceutical products and their processes is critical to the successful launch. Its success ensures that products of the highest quality are delivered to the patients along with meeting the business demands of the company. However execution of that transfer is complex involving the interactions of many disciplines across an organization. It depends both on the careful development, management, and transfer of technical and business knowledge along with the development of steps to define the formal transfer of that knowledge from R&D documents and systems to commercial manufacturing documents and systems.

Areas Covered in the Session :

  • The importance of technology transfer
  • The use of a technical review system to update and review technology knowledge obtained during drug product development
  • The use of a Product Strategy Review system to review important business aspects in preparation for transfer
  • Tools and Templates used for technology transfer
  • Interactive Q&A Session
Who Will Benefit:

  • Quality Departments
  • Regulatory Affairs Departments
  • Compliance Departments
  • Production Departments
  • Manufacturing Departments
  • Process Owners
  • Development Departments

FDB2301

Steven Laurenz

Steven Laurenz, Principal Consultant – BioPhia Consulting Inc., has over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. He is skilled in taking new products from early laboratory stage to successful manufacturing launch. He is an expert in integrating Quality by Design and risk management into product development. He has proven experience in establishing a Quality System for a R&D Quality Assurance organization.

Steven has headed product development departments at Abbott Laboratories and AbbVie Inc. and held leadership positions in numerous technical consortium.

Steven Laurenz holds an M.S. in Chemical Engineering from the Michigan State University

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance