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

Our Event Partners

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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


Clinical Supply



Pharma IQ Online Events | Who attends our events

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Pharma IQ Online Events | How it works


Step 1: Register
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Step 4: Watch the Event
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Gemma Mills
Head of Online

+44 207 368 9431