London, UK (May, 18 - 19, 2016)
Registration is now live to attend the 10th annual Clinical Trial Logistics conference taking place in London on 18th & 19th May 2016. The event will bring together leading industry professionals to discuss the latest regulatory developments, explore cost reduction, learn about logistical challenges in emerging markets, examine new innovations and examine best practices to ensure compliance of the new EU Clinical Trials Regulation which affects all parties in the clinical supply chain.
FEATURED EXPERT SPEAKERS INCLUDE:
* Graham McNaughton, Pharmaceutical Assessor, MHRA
* Elisabetta Carli, Head, Operations Clinical Vaccines Management, GlaxoSmithKline
* Tony Moult, Director, Clinical Supplies Ooperations, Daiichi Sankyo
* Geoffroy Bessaud, AVP, Anti-Counterfeiting Coordination, Sanofi
* Dawn Padfield, Director of Pharmaceutical Development and Clinical Supply, Norgine
* Elodie Fontaine, Clinical Trial Lead, Lundbeck
* Jasmine Hellwig, Senior Comparator Specialist, Merck Sharpe and Dohme
* Abdulkareem Ghanayem, Clinical Trial Operations Project Manager, Takeda
BENEFITS FOR ATTENDING:
* Gain key regulatory updated from Daiichi Sankyo and MHRA talking specifically on the development of the New EU Clinical Trials Regulation
* Discuss how to integrate forecasting and supply planning to an efficient clinical supply chain from GlaxoSmithKline
* Norgine presents how they ensure and maintain a successful contractor relationship
* Engage in discussions with Sanofi on visibility in the supply chain to fight counterfeiting
Book by 29th February to save ?400 and benefit from the best price.
Register online on http://www.clinical-trial-logistics.com/gate2biotech or contact +44 (0)20 7827 6184
www.clinical-trial-logistics.com/gate2biotech
Contact email: hdegracia@smi-online.co.uk
Contact number: +44 (0) 20 7827 6184
More: http://www.smi-online.co.uk/pharmaceuticals/uk/clinical-trial-logistic
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