We proudly present the return of the 10th annual
Clinical Trial Logistics to London in 2016. According to recent market research the clinical trial supplies market is expected to reach 1.2 Billion USD by 2020, with the logistics and distribution services segment accounting for the largest share of the market.
This rapid market growth is partnered with a huge change in the regulatory landscape. With the implementation of annexe 15 of the Good Manufacturing Practice (GMP) on the 1st October 2015, our 10th annual Clinical Trial Logistics event will provide the perfect platform to raise and discuss the challenges associated since the implementation.
Moreover, the development of the New EU Clinical Trials Regulation will impact all parties involved in the clinical supply chain - this conference will aim to address uncertainties and examine best practices to ensure compliance.
Our 10th annual
Clinical Trial Logistics event will bring together leading industry professionals to discuss the latest regulatory developments, explore how to reduce costs, learn about the logistical challenges in emerging markets and examine the latest innovations made on maintaining temperature in shipment.
Benefits of Attending
Join us today to:
- Gain key regulatory updates from leading competent authorities talking specifically on the development of the New EU Clinical Trials Regulation
- Discuss the latest innovations surrounding temperature control
- Join insightful discussions on; clinical trial logistics in emerging markets, forecasting, counterfeiting and many more!
- Engage in our interactive sessions and speed networking to solidify your learning experience amongst your peers
Speakers
- Abdulkareem Ghanayem, Clinical Trial Operations Project Manager , Takeda Pharmaceuticals
- Alan Dorling, Global Head - Pharmaceuticals & Life Sciences, IAG Cargo
- Alexandra Tsioni, Mgr, Clinical Supply Chain Study Lead, Teva Pharmaceuticals Ltd
- Amer Alghabban, Vice President Gxp Quality Assurance, Compliance Training , Karyopharm Therapeutics Inc.
- Amy Shortman, Consultant, Director, ASC Associates Ltd
- Anthony Moult, Director, Clinical Supply Operations, Daiichi Sankyo Ltd
- Dawn Padfield, Director of Pharmaceutical Development and Clinical Supply, Norgine Ltd
- Elisabetta Carli, Head, Operations Clinical Vaccines Management, GSK Italy
- Jasmin Hellwig, Senior. Comparator Specialist, Merck Sharp & Dohme
- Lis Hansen, Clinical Trial Supply Coordinator , Genmab A / S
- Rebecca Jackson, IVR/IWR Manager, Randomization & Trial Supply Services, Janssen
- Rocio Cuadtado, TSOM Leader , Sanofi
- Sanjay Nadarajah, Quality Director, Inglasia Pharma Solutions
- Terry Madigan, GDP Inspector, Inspectorate, Enforcement and Standards Division, MHRA
- Toby Hay, Global Sales Manager, FedEx HealthCare Solutions, FedEx
- Ulrike Kreysa, Vice President Healthcare, GS1
Please fill in your name and email to receive the conference agenda of this event.
The agenda is available as PDF under downloads at the right side of the page.
Venue
Holiday Inn Kensington Forum
97 Cromwell Rd, Kensington, SW7 4DN
London, UK
Who should attend
You should attend this event if you are a Director, Area Head, Chief Executive, CSO, or Vice President within the pharmaceutical or healthcare industry with responsibilities in the following areas:
- Supply chain
- Clinical Trials Operations
- Clinical Trial Supplies
- Logistics/ Distribution
- Regulatory Affairs
- Quality (Management/ Assurance/ Control/ GCP/ GMP)
Venue
Holiday Inn Kensington Forum97 Cromwell Road
London, United Kingdom
