Lesson series

Translation 3: Technology Transfer

Transfer of technology is an integral part of a product's life cycle and is subject to regulatory expectations, including risk-based and science-based process and method design. This module covers various aspects involved in planning, executing, and measuring the success of technology transfer initiatives. We explore types of technology transfer (scale-up and scale-out), planning for technology transfer and contract manufacturing organisation transfers. Upon completion, participants will gain an understanding of the roles and responsibilities of key stakeholders, knowledge requirements, regulatory considerations, risk management, execution phases, and measuring success.

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7 Topics

Across hours of online content

5 Case Studies

Direct from industry

3 Quizzes

Check your knowledge

1 Assessment

Complete the course

1 Q&A Webinar

Live session with a CBE Expert
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Supplementary Learning Materials

Videos, resources, useful reading, links and examples

Who is this course for?

CBE’s Translation Uplift program is designed to uplift participants knowledge in product realisation, technical elements that support translating an asset from R&D into the clinic and then ultimately as a commercial product. 

Senior Managers

The skill you need to become a real professional.

Researchers

Learn the tools used by the world's top professionals.

Regulatory Affairs

Boost your confidence, master "the field".

Meet your trainers for this course

Our trainers have decades of industry knowledge, technical expertise and practical experience across all aspects of the biopharmaceutical sector. 

Neil Radford

Course Trainer

Neil has nearly 30 years experience as a senior quality and operations leader in the Pharmaceutical and Medical Device industries, improving GxP Quality Systems and business processes across organisations in the US, UK, Europe, APAC, Latin America, the Middle East and beyond.

Maurice Parlane

Course Trainer

Maurice has significant international experience as a subject matter expert and specialist trainer in science and risk based approaches to manufacturing across the biopharmaceutical industry. He is a  professional engineer with over 30 years of experience in technical and consulting roles.