Product Showcases

Monday, September 24 | 12:45 PM – 01:30 PM

Location: PRODUCT SHOWCASE ROOM 1

The hallmark of Covance’s FSPx delivery engine is our focus on innovation, powered by our ability to deliver unique technology-based assets that assist in adding value to our customers. In our relentless pursuit to provide best-in-class services, we bring customized technology assets that enhance our customer experience.

These applications are powered by our Innovation Centre of Excellence, which has continuously delivered tools and frameworks that drive measurable operational improvements. Some of the key initiatives taken up by this CoE are related to EDC Accelerators, Test Data Simulation, and Statistical Programming Workflow as well as advancements in Reporting & Analytics.

Monday, September 24 | 12:45 PM – 01:30 PM

Location: PRODUCT SHOWCASE ROOM 2

Clinical Data at Your Fingertips: Using Modern Browser Techniques to Streamline Data Management

Browser technology has evolved since the early days of developing web based EDC, for example the introduction of HTML5. Standards have also been developed and adopted to provide a more consistent and intuitive user experience across web sites. Our demo will show how we have incorporated these into a modern UI for Data Management.

Monday, September 24 | 03:15 PM – 04:00 PM

Location: PRODUCT SHOWCASE ROOM 1

SCDM Abstract: Three Ways to Combat Clinical Data Management Challenges

As the flood of new clinical trial data sources rapidly grows, so do the challenges around clinical data quality, traceability and oversight.

In this session, Oracle Health Sciences’ Senior Director of Product Strategy, Greg Jones, dives into a recent study that reveals insight into these current clinical data management challenges, and presents three practical ways the industry can combat these challenges in order to bring new and innovative therapies to market faster, and at lower cost.

Monday, September 24 | 03:15 PM – 04:00 PM

Location: PRODUCT SHOWCASE ROOM 2

The Benefits of a Completely Electronic Data Collection Platform: eConsent, eSource, ePRO, and EDC

The cloud has been a transformative technology for every aspect of our personal and professional lives. But while clinical trials have not adopted cloud technology as rapidly as other industries, the benefits are getting harder and harder to ignore. Decentralized workforces, trials that span the globe, and an increasing number of stakeholders are making trials more complex to manage. We will show, complete with demos, how an integrated, cloud-based data collection platform can reduce timelines, improve patient retention, simplify management, and much more.

Tuesday, September 25 | 10:30 AM – 11:15 AM

Location: PRODUCT SHOWCASE ROOM 1

Built on a modern unified clinical platform, Veeva Vault EDC allows you to run the trial you want, not the trial your technology limits you to. Quickly deploy studies in weeks, not months, and make in-flight amendments without migrations or downtime. The ability to integrate and maintain complete and concurrent trial data, including non-CRF data, provides real-time insights and dramatically improves productivity.

Tuesday, September 25 | 10:30 AM – 11:15 AM

Location: PRODUCT SHOWCASE ROOM 2

IBM Clinical Development is a unified solution positioned to Transform the Clinical Trial industry by leveraging cognitive capabilities, data assets, IoT and EMR/EDC integrations. Designed to optimize protocol development, enhance patient/site recruitment and digitize clinical trial processes; IBM Clinical Development can help reduce the time and cost of clinical trials and help life science organizations bring therapies to market faster to benefit patients.

Tuesday, September 25 | 12:45 PM – 01:30 PM

Location: PRODUCT SHOWCASE ROOM 1

For decades, integration between EHR and EDC systems has been seen as the “holy grail” to optimize clinical research. Finally, key technologies and standards are now making such integration a reality. The presenter will explain how SMART and FHIR on the EHR side and CDISC CDASH and ODM on the EDC side allow for integration — without protocol-specific custom coding.

The speaker will describe the solution developed by Clinical Pipe and implemented successfully in oncology clinical trials across multiple academic clinical trial centers. Clinical Pipe can integrate with any SMART on FHIR EHR system and connect to any EDC system with a real time API. As of July 2018, the application integrates the 4 leading EHR systems and export data in real time to Medidata Rave and Protocol First EDC. The speaker will also address downstream operational impacts of acquiring data “automatically” from the EHR

Tuesday, September 25 | 12:45 PM – 01:30 PM

Location: PRODUCT SHOWCASE ROOM 2

Beyond eConsent: How a Unified Platform can simplify and streamline Clinical Development with a Patient Centric Approach

Abstract: Adopting an eConsent solution comes with many benefits by itself, less burden on patients and sites, improved learning and retention of trial information and better overall patient retention. But more benefits are unlocked when eConsent is used in conjunction with a platform that allows patient data to seamlessly flow into RTSM and EDC capabilities.

Join us for this live demonstration to learn how Medidata platform streamlines the patient experience while reducing study timelines by allowing patients to enroll electronically, automatically triggering randomization and kit procurement, so patients can fully participate in the trial from in their initial visit.