Unsurprisingly, with the introduction of these regulations comes challenges and change of practice - how will clinical supply chain professionals change their current strategy and what actions need to be taken to ensure they are compliant in the next year. In addition to this, questions are raised on what practical implications will the new regulation have on clinical supply chains and what flexibility will there be in regards to enforcement?
Following an explosion of interest from our established community of Clinical Supply Directors, we are proud to present the 7th annual Clinical Trial Supply Europe event, a supreme opportunity for pharma and biotech companies to benchmark their existing and future clinical supply chain strategies with 150+ of your peers to ensure they are innovating their packaging and labelling correctly first time and effecting remaining compliant with the regulations.
Learn from a panel of senior Clinical Supply Chain Directors including:
- Claudio Lorck, Associate Director Clinical Product Supply EU, QP Lead, Abbvie
- Alice Stephan, Global Clinical Supply Coordinator, Roche
- Thomas Thoma, Head Clinical Trials Supply, Teva Europe
- Simon Denegri, National Director for Patients and the Public and Chair, National Institute for Health Research
- Lesley Holt, Director of Clinical Supplies, Mundipharma
>> The full event programme is available to download here
The Clinical Trial Supply Europe conference will be taking place in London on 23rd - 25th January. Find the full programme and registrations details on http://www.clinicalsupplyeurope.com, phone +44-(0)207-036-1300 or email email@example.com
Media Contact: Rumina Akther, Trainee Marketing Manager, IQPC: firstname.lastname@example.org or call +44-(0)207-368-9442
Press are invited to attend this important industry summit, if you would like to a complimentary press pass please email Rumina Akther on email@example.com
SOURCE IQPC UK