Leveraging data, artificial intelligence, flexible trial design and digitization to improve clinical trial success and reduce the cost of failure
Clinical trials remain one of the most costly and difficult aspects of getting a drug to market. A newly discovered drug will take a median of nine years before it is approved for the market at an average cost of $2.6bn.
The cost of failure is high, and there are several common fracture points in the process including not recruiting enough patients, patients dropping out during the course of the trials, poor data governance and collection as well as unintended side effects.
With that in mind, Clinical Trial Design 2020 will be focused on improve the chances of success, and minimise the cost of failure by:
- Leveraging Artificial Intelligence to improve patient recruitment, by matching the right patients to the right trials
- Using data to make faster go/no go decisions
- Engaging in adaptive and flexible trials in order to improve their responsiveness and chances of ultimate success
- Enhancing integration and digitization in order to improve transparency and data sharing
- Utilizing mobile technology in order to increase medication and protocol adherence
- Understanding how to use IoT and continuous patient data to provide real time monitoring and feedback
5 Reasons to Attend
Hear the best case studies from across the globe
No travel costs or time out of the office necessary
Access the content on demand and watch in your own time
Assess the latest technological innovations
It is 100% free to attend
2020 Speakers
Elizabeth George
Director, Clinical Trials Diversity
GSK
Musaddiq Khan
Director, Clinical Program Operations
Eli Lilly
Kim Hawkins
Global Head CSO Project Leaders
Sanofi
Gareth Powell
Business Development Officer and Patient Engagement Project Lead
NIHR Clinical Research Network
Terttu Haring
Global Head for Clinical Digital Innovation
Sanofi
Keri Mcdonough
Lead, Advocacy and Patient Relations
Syneos Health Communications
Poonam Pattni
Senior Associate, Global Clinical Trial Disclosure
Eisai
Paul O’Donohoe
Scientific Lead, eCOA and Mobile Health
Medidata Solutions a Dassault Systèmes Company
Fiona Maini BSc. MSc.
Principal Global Compliance and Strategy
Medidata Solutions a Dassault Systèmes Company
Rosamund Round
Vice President, Patient Innovation Center and Decentralized Trials
Parexel
Our Event Partners
Who should attend?
The event has been designed for Directors / Heads / General Managers and VPs of
Clinical Supply Technology
Clinical Trial Design
Clinical Operations
Scientific Operations
Research
Clinical Supply
Development
Therapeutics
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Step 1: Register
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This will be dispatched upon registration and will contain information like how to login
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