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Modern drug development – keeping your nonclinical program on track

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If you have a question about this talk, please contact Emma Neave.

*pre-registration required, see event info for details*

Join us to discuss the challenges in designing and executing a nonclinical development program

Examples and case histories on both small and large molecule therapeutics will be discussed demonstrating how novel approaches in design and the management of unexpected outcomes can help keep your nonclinical development program on track to meet your clinical and regulatory timelines.

Following two presentations there will be a panel discussion where delegates will have the chance to have their real questions answered by an expert. The event concludes with an industry-leading expertise workshop, where delegates will be exploring ways in which cross-company collaboration could fundamentally change businesses for the better.

Locations

Wednesday 4 July, 3:30pm-6:30pm – Bradfield Centre, 184 Cambridge Science Park, Milton Road, Milton, Cambridge, CB4 0GA

Thursday 5 July, 3:30pm-6:30pm – Babraham Research Campus, Cambridge, CB22 3AT

Friday 6 July, 3:30pm-6:30pm – Oxford Science Park, Magdalen Centre, Robert Robinson Avenue. Oxford, OX4 4GA

Monday 9 July, 3:30pm-6:30pm – Crowne Plaza Hotel, 100 Cromwell Road, London, SW7 4ER

Tuesday 10 July, 3:30pm-6:30pm – Holiday Inn – Camden Lock, 30 Jamestown Road, London, NW1 7BY

Agenda

  • 3:30pm – Registration and arrival refreshments
  • 4:00pm – Welcome
  • 4:05pm – Drug development – expect the best, plan for the worst, and prepare to be surprised! Dr. Robert Turcan, Head of Regulatory Affairs and Program Management, Envigo
  • 4:45pm – Identifying, addressing and smoothing the bumps in the road to successful non-clinical development, Dr. Kirsty Harper, Head of Biologics, Envigo
  • 5:30pm – Panel session
  • 6:00pm – Industry-leading expertise workshop, Rachel Buckley, VP Customer Experience, Envigo
  • 6:30pm – Event close

Why attend?

  • This meeting is aimed at biotech companies planning their nonclinical package of work, and looking to progress to their first clinical studies
  • Delegates will hear from industry experts presenting insightful and informed scientific content through best practice and case study sessions, sharing nonclinical drug development trends that will help delegates get to market sooner
  • The format of the event ensures delegates have the opportunity to have their real questions answered by an expert
  • Delegates will receive a post-event report highlighting key discussions from the panel sessions taking place across the five venues, as well as a summary of the needs discussed in the scientific expertise workshops across the five venues

Pre-registration is required, please visit our registration page

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