The ability to use BYOD mobile apps in studies to conduct eConsent, ePRO, medical device reported outcomes, medical record integration, telehealth and more is enabling research to be carried out with less friction for patients, more continuously during a study and with potentially fewer in-clinic visits.
This session will review how virtual / remote patient research approaches work, how our industry (pharma, regulators, academic researchers) is supporting this change and what attendees can do to adopt this approach in support of their career growth.
Understand what virtual/remote patient research is and how it is used in research studies.
Articulate the operational benefits/risks to support adoption of this approach in research studies.
Realize the industry impact and pursue adding this approach to their career expertise.