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How do we redesign our clinical trials so they become a place where we learn about our customers, sites and their interaction with our products?

  • 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

Join the most pioneering clinical minds at 2017’s event

Murray Stewart
Murray Stewart

GSK

Chief Medical Officer

David Christie
David Christie

Amgen

VP Research and Development Informatics

Lisa Egbuonu-Davis
Lisa Egbuonu-Davis

Sanofi

VP Global Patient Centred Outcomes and Solutions

Brooks Fowler
Brooks Fowler

AbbVie

Global Head of Data Sciences

Melva Colvington
Melva Colvington

Sanofi

Senior Director, Head of Field Based Medical Strategy,

Pablo Lapuerta
Pablo Lapuerta

Lexicon Pharmaceuticals

Executive Vice President and Chief Medical Officer

Dawn Furey
Dawn Furey

Merck

Executive Director, Head of Global Operations

Mohammed Ali
Mohammed Ali

Janssen

Director, R&D Operations and Innovation Leader

Alice Donnelly
Alice Donnelly

Bristol-Myers Squibb

Clinical Planning and Execution Lead, Global Clinical Operations, R&D

Aman Thukral
Aman Thukral

AbbVie

Assistant Director, Strategy and Innovation

Matthew Bryant
Matthew Bryant

Amgen

Director Patient Engagement Technology

Sarah Krüg
Sarah Krüg

CANCER101

CEO

Download the detailed event brochure

Complete speaker line-up • Program for all tracks & sessions • Audience breakdown

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

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Caitlin Champion

Caitlin Champion

Global Project Director
eyeforpharma

Phone: +44 207 375 7190

Email: caitlin@eyeforpharma.com