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Join the most pioneering clinical minds at 2017’s event

Aditi Kumar
Aditi Kumar

Amgen

Executive Director, Clinical Systems

Brooks Fowler
Brooks Fowler

AbbVie

Global Head of Data Sciences

Melva Colvington
Jyotsna Mehta

Alkermes, Inc.

Director, Economics Value Evidence and Outcomes

Pablo Lapuerta
Pablo Lapuerta

Lexicon Pharmaceuticals

Executive Vice President and Chief Medical Officer

Sam Hume
Sam Hume

CDISC

Head of Data Exchange Technologies

Kannan Natarajan
Kannan Natarajan

Pfizer

Global Head of Biometrics and Data Management

Aman Thukral
Aman Thukral

AbbVie

Assistant Director, Strategy and Innovation

Sarah Krüg
Sarah Krüg

CANCER101

CEO

Mohammed Ali
Mohammed Ali

Janssen

Director, R&D Operations and Innovation Leader

Robin Heiskell
Robin Heiskell

Bristol-Myers Squibb

Associate Director, Strategic Clinical Relationships

Christopher Pitcherella
Christopher Pitcherella

Teva

Director, Clinical Trial Innovation

Raj Nimmagadda
Raj Nimmagadda

Novartis

Director, Global Head - Data Sciences & Standards, Analytics

Re-design clinical trials so they don’t just determine safety and efficacy but also provide key information about patient experience of a drug in order to bring better products to market, quicker.

  • From cost-center to revenue-generator: turn your clinical trials from an expensive burden into a differentiating asset

  • Minimise the need for post-marketing trials: incorporate live patient data into your processes to improve the quality of products before launch

  • Improve quality of data and save time by automating and streamlining processes for sites

  • Enhance patient engagement and retention with new technologies that reduce the burden

  • Build smarter, more effective strategies by combining big data with sophisticated analytics and real-time feedback

Purchase the Post-Conference Materials

Event Presentations • Event Audio • On Demand Subscription

Usable patient feedback shouldn’t wait for after a product launch. It’s time to embrace data.

As patients become more engaged in healthcare decisions, they’re generating huge amounts of data. If you’re not collecting this feedback, analyzing it and putting it to good use, you’re missing an opportunity to redefine your products. During the 2nd annual Data and Technology in Clinical Trials Summit, you’ll learn how to focus on and make use of the most important data at your disposal to create better products with accurate dosage information from day one.

By accessing the data streams at your fingertips, you’ll ensure that your trials don’t just efficiently determine safety and efficacy. They’ll also provide you with key information you need to bring better products to the market.

The end result will be more efficient trials, shorter and more cost-effective development processes, and a product that launches with the benefit of genuine, real-world feedback to help you position it correctly. In short – it’ll give you a real competitive advantage.

Join us to learn from real-world implementations of new data gathering and analysis methods, and to see how new technology and data can be used to lead pharma forwards into a future filled with cost-effective trials, high quality products and satisfied customers.

Our Track-Record of Proven Success

83% call our sessions essential
94% say they'll return next year
97% rated the program very well done

What our Delegates are saying

Purchase the Post-Conference Materials

Event Presentations • Event Audio • On Demand Subscription

Caitlin Champion

Caitlin Champion

Global Project Director
eyeforpharma

Phone: +44 207 375 7190

Email: caitlin@eyeforpharma.com