TORONTO (PRWEB) February 04, 2020 -- Finding the right patients and the right clinical trial sites can be a challenge for any clinical trial. Coupled with the competition for qualified and available sites within a specific therapeutic area, drug development sponsors may also face a shortage of qualified patients to study.
On Tuesday, February 25, 2020 at 11:00am CST/China (12:00pm JST/Japan, 12:00pm KST/Korea), join Covance’s Michelle Jones, MSc, Senior Director of Clinical Informatics and Bireshwar Saha, M.Pharm, Senior Director and Global Head of Clinical Programming & Analytics in a live webinar to learn what sponsors can do to optimize their trials.
The webinar will focus on the use of real-world data to help sponsors design more patient-centric study protocols that are optimized to patients’ needs and reduce the burden of participation. Patient data can also help sponsors pinpoint new geographical locations of patient populations and match those patients to qualified sites by looking beyond historical performance and accounting for disease incidence and protocol-evaluable patient density information. Taken together, these data can increase the predictability of recruitment timelines — a key factor in improving the overall efficiency of a trial.
Additionally, the webinar will cover different study designs such as decentralized hybrid/virtual trials to enable patient-centric drug development.
This webinar will be suitable for senior level directors and managers working in clinical operations, business or clinical development, procurement and other related departments.
For more information or to register for this event, visit Applying Data Analytics and a Decentralized Trial Platform for More Efficient Patient-Centric Trials.
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Mira Nabulsi, Xtalks, http://www.xtalks.com, +1 (416) 977-6555 x 400, [email protected]