- This event has passed.
Event Date: March 21, 2018, 12:00-1:00pm EST
Registration Deadline: March 20, 2018
Member: $15 | Nonmember: $75
This program is accredited to provide 1.0 ACRP or CBRN contact hours.
Member: $0 | Nonmember: N/A
Virtual / remote patient research is rapidly expanding from innovative pilots to a standard approach in clinical research. This growth trend is expected to see exponential growth from 2018 – 2020 and impact how research studies are conducted.
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.
Our 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.
Upon completion of this Webinar, attendees should be able to:
1. Understand what virtual/remote patient research is and how it is used in research studies
2. Articulate the operational benefits/risks to support adoption of this approach in research studies
3. Realize the industry impact and pursue adding this approach to their career expertise
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