Plymouth Meeting, PA – February 28 2017: CRF Health, the leading global provider of patient-centered eSource technology and service solutions for the life sciences industry, has opened registration for the 2017 eCOA Forum. Focusing on ‘The Electronic Clinical Trial’, the event will take place from 10-11 May 2017 at the Hotel Pullman in Basel, Switzerland. The free educational event will address the continuous challenge of aligning high quality and efficient migration and integration of data collection through eSource, wearables and BYOD. Conference details and registration information can be found at www.ecoaforum.com.
The 2017 eCOA Forum is CRF Health’s 6th annual meeting that focuses on advancing the use of eCOA for patient data collection in clinical trials. Bringing together leading thinkers in health economics and outcomes research (HEOR), data management and clinical operations, the conference is open to first time eCOA adopters as well as advanced users to discuss real-world challenges, share patient-centric innovations and to keep up-to-date on the latest eClinical innovations.
The two-day event brings together like minded professionals to address trends and topics in eCOA, including eCOA for adaptive trials, equivalence testing, data & analytics, and eConsent. The eCOA Forum will feature 16 sessions presented by a range of industry experts, as well as two interactive workshops. Amongst the list of scheduled speakers are:
- Anders Morten, TriTiCon
- Bill Byrom and Willie Muehlhausen, ICON
- Chris Fidyk and Paul Wicks, PatientsLikeMe
- Dagmara Kulis, EORTC
- Michelle White, Quality Metric
- Rebecca Prince, Corporate Translations Inc.
- Tunde Nagy, Stefanini
“Clinical trial technology continues to rapidly move forward, bringing with it changes that must be explored. Ensuring patient centricity and allowing seamless patient participation in clinical trials is also a major priority”, commented CRF Health’s CEO, Rachael Wyllie. “Our 6th annual eCOA Forum will discuss what these trends will mean for the industry, and how organizations in the space can prepare. It is also a great platform for individuals working in all aspects of clinical research and data collection to network and discuss best practices of eCOA in Clinical Trials.”
For further information on CRF Health, please visit http://www.crfhealth.com.
About CRF Health
CRF Health is the leading provider of patient-centered eSource technology and service solutions for the life sciences industry. With experience in more than 800 trials, over 100 languages and across 74 countries, CRF Health’s TrialMax® platform consistently demonstrates the industry’s highest data accuracy, patient and site compliance, and patient retention.
CRF Health’s eSource solutions improve trial engagement by fitting into the lives of patients and seamlessly integrating into sites to maximize protocol compliance. The integrated TrialMax platform includes eCOA solutions for collecting PROs (Patient Reported Outcomes), ObsROs (Observer Reported Outcomes), and ClinROs (Clinician or Rater Reported Outcomes), PerfOs (Performance Outcomes) and features TrialConsent™, an electronic solution for collecting informed consent in clinical trials.
Contact: email@example.com, +1 267.498.2350
About the Author