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Conference Documentation: Clinical Trial Logistics

Conference Documentation: Clinical Trial Logistics

The clinical trial logistics world is accelerating rapidly with trials now occurring in more than 13 strategic and emerging markets with eyes on the improvement of global health and patient care. The demand for clinical trial supply and logistics has gone global with increased outsourcing, with a predicted forecast of $14.3bn by 2017. The market demand has impacted supply chain management and our aim at the SMi Group is to provide a conference that will enable key opinion leaders to discuss, assess and analyse supply chain security, temperature monitoring and reflect on the globalisation of clinical trial logistics.


Day 1
8:30
Registration & Coffee
9:00
Chairs Opening Remarks
Tony Wright, Managing Director, Exelsius Cold Chain Management
9:10
A risk based monitoring approach for non-cold chain temperature-sensitive IMP products
Tim Wood, Technical Service Manager, GlaxoSmithKline
9:50
FOCUS SESSION - Simulation based decision-making for Clinical Trial Supply
Sebastien Coppe, Head of Consulting Group, N-SIDE
10:30
Morning Coffee
11:00
Predictive analytics in risk-based monitoring of trial operations
Vladimir Anisimov, Senior Strategic Biostatistics Director, Quintiles
11:40
KEYNOTE ADDRESS: Understanding labelling of different clinical trial products
12:20
Networking Lunch
13:30
GS1 Standards: Relevant to the global pharmaceutical supply chain?
Janice Kite, Tracibility Director Healthcare , GS1
14:10
ROUND TABLE DISCUSSION - How to integrate new technologies into IT-Systems for Clinical Logistics
Nimer Yusef, CEO, Trial-Brain
14:50
Afternoon Tea
15:20
Challenges in air freighting Clinical Trial Products across a global network
Alan Dorling, Global Head - Pharmaceuticals & Life Sciences, IAG Cargo
16:00
ROUND TABLE DISCUSSION - Supply Chain Logistics
Tony Wright, Managing Director, Exelsius Cold Chain Management
16:40
Chairs Closing Remarks and Close of Day One
Tony Wright, Managing Director, Exelsius Cold Chain Management
Day 2
8:30
Registration & Coffee
9:00
Chairs Opening Remarks
9:10
Harmonisation throughout the distribution process from start to finish
9:50
KEYNOTE ADDRESS - An efficient supply chain maintained!
Sylvie Noirault, Project Head, Clinical Supplies, Sanofi R&D
10:30
Morning Coffee
11:00
Pharma Supply Chain: Minimising Risk by Maximising Security
Tom Harrington , Sales and Distribution Manager , Cryopak Europe
11:40
Case Study 1: Partnerships in supporting clinical trial logistics from a pharma perspective
Beth Freeman, Senior Program Manager, Global Clinical Trial Supply Chain, Takeda
12:20
Case Study 2: Partnerships in the clinical trial supply chain
Tony Heeley, Director, Business Development CTSL, PAREXEL
13:00
Networking Lunch
14:00
Joint Case Study: Global Certification: How to meet challneges and requirements of the pharmaceutical industry
Andrea Gruber, Manager Business Process & Standards, IATA
14:00
Joint Case Study: Global Certification: How to meet challneges and requirements of the pharmaceutical industry
Brice Bellin, Healthcare Regional Manager - Europe, SDV
14:40
Panel Discussion - Partnering in Clinical Trial Supply
Andrea Gruber, Manager Business Process & Standards, IATA
14:40
Panel Discussion - Partnering in Clinical Trial Supply
Beth Freeman, Senior Program Manager, Global Clinical Trial Supply Chain, Takeda
14:40
Panel Discussion - Partnering in Clinical Trial Supply
Tony Heeley, Director, Business Development CTSL, PAREXEL
15:20
Chairs Closing Remarks and Afternoon Tea

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