Industry Events

CBI's Interactive Response Technologies in Clinical Trials 2016

October 25, 2016October 26, 2016
Hilton at Penn's Landing, Philadelphia, PA

CBI's Interactive Response Technologies in Clinical Trials conference is the industry's premier event for clinical operations and supply chain, and clinical systems professionals. Be sure to join us Tuesday, October 25 from 1:45 - 3:05 PM, as Medidata's Balance Managing Director, Wade Wirta will be speaking to the RTSM Model and dive into how you can improve your study when there is real-time data available. For more information on Balance and the Medidata Platform, we invite you to stop by our booth during the show. To register for the event, please visit the CBI event website. Looking forward to seeing you in Philly!

Clinical Data, Real Data, Open & Big Data

November 7, 2016November 8, 2016

Medidata is a Gold Sponsor at the The 21st General Assembly of the Association DMB. This one day conference will be held Monday, November 7, 2016 from 09:00 to 18:00 at the Cité Universitaire in Paris. To learn more about the event, just visit the DMB website.

Partnerships in Clinical Trials 2016 - Vienna, Austria

November 16, 2016November 17, 2016
Vienna, Austria

Medidata is excited to participate in this year’s “Partnerships in Clinical Trials” conference in Vienna, Austria, 16–17 November. The conference brings together pharma and biotech sponsors and providers with the common goal of strengthening partnerships, and this year will focus on the reforms, challenges and innovations transforming clinical research.

Hear from industry thought leaders from pharma, CRO’s, and regulatory bodies in a discussion moderated by Medidata on “How Data Quality is Impacting Clinical Trials and Patient Experience”, which will cover the following topics:

  • The (un)repeatability of trial results: it’s been reported that less than 50% of clinical trial results can be successfully replicated, meaning many results are not true. How does data, good or bad, play a role in these results and what’s the impact on patients once these drugs are on the market? Does bad data quality impact patients enrolled in studies?
  • A regulator’s perspective on data quality: How does the FDA and the EMA view data?
  • A new paradigm for data quality management: machine-learning algorithms are able to scrub data, reducing the need for costly and ineffective edit checks. What does this mean for data managers and time to market for new drugs?

Additionally, visit us at booth 159, where we’ll be giving interactive demonstrations of the solutions within the Medidata Clinical Cloud™, our industry-leading platform for clinical development. If you haven’t yet registered and are interested in attending, visit the PCT 2016 website to register. 


Dinner and Dialogue - Enhancing Data Quality Oversight Through Analytics and Machine Learning

November 8, 2016November 9, 2016

Medidata is hosting a roundtable dinner on leveraging analytics and machine learning to help sponsors comply with ICH E6 guidance while providing a new level of precision in data quality oversight. We hope you will join us in Philadelphia or London for this important roundtable series.

Register now for a dinner near you.

*This subject matter is appropriate for sponsor and CRO attendees at a director level or above. 

Is Site Payment Escrow a Thing of the Past? YES!

November 10, 2016

Join us on November 10, at 12:30 am BST, as our experts discuss the paradigm shift in payment tracking from excel or home-grown systems to more commercial, turn-key technology. With a new escrow-free process and EDC-driven payment process, Sponsors and CROs alike are easily able to project, trigger, calculate and disburse payments in any currency quickly and accurately. The cash remains with the sponsor, the sites receive their payments and the trial progresses seamlessly. It is the proverbial win-win-win for all. Please visit our registration page for more information.