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Pharmaceutical Event: Impact of the EU Regulation (536/2014) (G3) | PharmiWeb.com
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Impact of the EU Regulation (536/2014) (G3)

Impact of the EU Regulation (536/2014) (G3)

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Who should attend?

Clinical researchers with at least one year of experience, who wish to explore the impact and wider application of the new EU Regulation for Clinical Trials on their current practices.

Details

The 2001 Clinical Trials Directive (2001/20/EC) has been criticised by patients, researchers and industry alike for its disproportionate regulatory requirements. High costs and a lack of harmonisation of the applicable rules necessary for multinational clinical trials have contributed to a significant decline in the number of clinical trials in the EU – a reduction of about 25% in the last few years.
The new EU Clinical Trials Regulation is due to be enacted in 2016 and will replace the 2001 Clinical Trials Directive (CTD) (2001/20/EC). The Regulation aims to restore the EU’s competitiveness in clinical research and the development of new and innovative treatments and medicines by cutting red-tape and bringing patient-oriented research back to Europe.
The regulation includes rules for clinical trials which are conducted outside the EU but referred to in a clinical trial application within the EU. For such trials, the rules call for compliance with regulatory requirements at least equivalent to those in the EU, including rules on transparency.
In this highly interactive course, we explore the changes proposed by the regulation and how they will impact our current practices in conducting global clinical trials.

Prices

Member 450 GBP, Non Member 550 GBP, Discounts for those working in the NHS or Academia

Contact

James Christianson
office@icr-global.org.uk

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