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Cell & Gene Therapy International Europe

Savings Deadline Expires In:

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2-4 December 2024
Convention Centre DublinDublin, Ireland
2-4 December 2024
Convention Centre Dublin,
Dublin, Ireland

Real-World Insights. Trusted Resources. Novel Solutions.

NEWS FLASH: BRAND NEW 2018 CONTENT

Manufacturing and Process Development – Analytical Strategies, QbD and Cost of Goods

  • Get top tips on monitoring quality across the process with automated analytics
  • Dive into costs of goods calculations and considerations
  • Hear from Allogene, Cellectis and Shire

Facility Design, Manufacturing Networks and End to End Solutions for Commercial Success

  • Keep abreast of affordable and scalable manufacturing strategies
  • Insourcing vs. outsourcing- What's the right path for you?
  • Top tips from Pluristem, Unum and CCRM

Clinical Development for Cell, Gene and Immunotherapies

  • Get the latest on development pipelines – discover NKs, TILs, MILs, TCRs and more...
  • Pick up knowledge on process validation and supply chain strategies in the clinic
  • Insights from MPA, TC Biopharm and GenSight

Logistics, Supply Chain, and Cryopreservation

  • Immerse yourself in vein-to-vein supply chain and transportation considerations

  • Explore the effects of freezing and thawing on cell viability

  • Feedback from Kite, Ossium and Celyad

Additional Learning Opportunities: Pre - conference workshops

  • NEW FOR 2018: Raw Materials Focus Day
  • Comparability for ATMPs
  • Case studies from Novartis, NIBSC and Juno

NEW FOR 2018: Visit Sanquin's GMP Facility

  • 2 hour exclusive tour of their new, state of the art, facility
  • Blood bank, reagents, diagnostics and the cell therapy lab
  • Places are capped at 25 (only valid for those attending raw materials session)

Cell Therapy Manufacturing and Gene Therapy Plenaries

Day 1: Opening Plenary

Start the day with a strategical discussion on how we should be designing our manufacturing facilities of the future and our delivery into healthcare

  • How could innovation lead to a more flexible process and control across supply chains?
  • What is needed from industry to make it possible to treat multiple patients?

Day 1: Closing Plenary

Come together at the end of Day 1 for an inspirational talk .... we want to make it special so are still working towards getting the best speaker for you...

Day 2: Morning Plenary

Our final plenary examines the current regulatory hurdles facing those in the industry…

  • What are the current regulatory challenges in ATMP development
  • A closer look at the proposed global changes to requirements surrounding GMP inspections – expectations and impact