Skip navigation

BioWednesday London: Avoiding Pitfalls and Maximising Value in Clinical Trials

14:45 - 21:00

Marsh Ltd, Tower Place East, London, EC3R 5BU
03 May 2017

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.


Principles of Good Clinical Practice

14.45 – Registration over Tea and Coffee

15.15 – Presentations Including:

The CRO perspective – Speaker tbc, Chiltern

16.25 – Coffee Break

16.40 – Presentations Including:

From a Site’s Perspective: Optimising GCP and Subject Enrolment
Liam Eves, hVivo

European Medicines Agency Pre-Approval GCP Inspections: Learning From Past Experience
Martin Moxham, Clinical Network Service

17.45 – End of Afternoon Session / Networking over Tea and Coffee

Avoiding Pitfalls and Maximising Value in Clinical Trials

18.30 – Introduction

18.40 – How to ‘Risk Map’ Clinical Trials

19.00 – Panel discussion around best practice and lessons learned from planning and conducting clinical trials

Julie Simmonds, Panmure

Linda Summerton, Immodulon Therapeutics

19.30 – Closing Remarks

19.45 – Networking over Drinks and Canapés

21.00 – End 

Members: free 
Non-members: £50 (plus vat) 
Academics: please contact

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