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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! 

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Venue
IQPC Ltd

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

Organised by
IQPC UK
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