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Trial Master Files

12 September 2016 08:00 - 14 September 2016 17:00, London, United Kingdom


Introduction
Are you looking to:

Represent a complete TMF and ensure inspector readiness? - The Danish Medicines Agency present a case study to ensure you are inspection ready

Effectively manage internal and external correspondence? - UCB share their expertise

Successfully convert to a cost-effective eTMF system? - Mitsubishi Tanabe share their expertise 

Ensure positive CRO oversight that ensures TMF completeness, quality and timely delivery? - Covance and Biomarin share their two differnt perspectives 

Ensure efficiency with a perfected interoperability strategy? - Phlexglobal offer their insight

In this 100% case study and discussion based event, we are joined by industry experts from across pharma and regulatory bodies, who will help you solve all of your TMF challenges! 
Venue
IQPC Ltd

IQPC Ltd, 129 Wilton Road, London, SW1V 1JZ, United Kingdom

Organised by
IQPC UK
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