Skip navigation

BioWednesday London: Avoiding Pitfalls and Maximising Value in Clinical Trials

14:45 - 21:00

Location:
Marsh Ltd, Tower Place East, London, EC3R 5BU
Date:
03 May 2017
 
To view the report following this event, please click here: Minimising Risk in Clinical Trials.




This event will review the different aspects to take into consideration regarding Good Clinical Practice that should be embedded throughout the planning and implementation of any clinical trial to ensure patient safety, avoid regulatory breach and to maximise short and long term prospects of a clinical pipeline.

Good Clinical Practice will be reviewed from different perspectives, including experience sharing from mid stage biotech and pharmaceutical companies and experts in regulatory affairs, clinical research and insurance. 

This event should appeal to any biotech company wanting to get a review of clinical trials best practice or anyone involved in clinical trials with interest in widening their knowledge and network.

Programme:

Principles of Good Clinical Practice

14.45 – Registration over Refreshments

15.30 – Welcome from the Host and One Nucleus
Simon Thompson, Marsh
Click here to view the presentation
Aline Charpentier, One Nucleus

15.40
– Good Clinical Practice – ValiRx Perspective 
George Morris, ValiRx
Click here to view the presentation

16.05 – Clinical CRO Selection and Management - Gaining Maximum Value
Peter MacLennan, TCRS
Click here to view the presentation

16.25 – From a Site’s Perspective: Optimising GCP and Subject Enrolment
Liam Eves, hVivo
Click here to view the presentation

16.50 – Coffee Break 

17.05 – European Medicines Agency Pre-Approval GCP Inspections: Learning From Past Experience
Martin Moxham, Clinical Network Service
Click here to view the presentation

17.30 – FDA Readiness
Gordon Elger, UL Compliance to Performance
Click here to view the presentation

17.55 – Closing Remarks

18.00 - Networking over Refreshments


Avoiding Pitfalls and Maximising Value in Clinical Trials


18.30 – How to ‘Risk Map’ Clinical Trials
Andrew Tamworth, Marsh

Click here to view the presentation


18.50
– Panel Discussion: Best Practice and Lessons Learned from Planning and Conducting Clinical Trials

Chair:
Julie Simmonds, Panmure Gordon

Panel:
Joseph Chiasa, Transcrip
Gordon Elger, UL Compliance to Performance
Peter MacLennan, TCRS

19.30 – Closing Remarks

19.45 – Networking over Drinks and Canapés

21.00 – End 


Prices
Members: free 
Non-members: £50 (plus vat) 
Academics: please contact aline@onenucleus.com

Title: BioWednesday London: Avoiding Pitfalls and Maximising Value in Clinical Trials
Start: 2017-05-03 14:30:00Z
End: 2017-05-03 21:00:00Z