The Age of eSource: Modernizing Clinical Trials
A Free CenterWatch Webinar
Sponsored by Medrio
If you would like to view the recording please register.
What do you know about eSource and the problems it can solve?
Implement eSource and you’ll see your productivity increase. Data quality will be improved, timelines will shrink and the financial savings will be significant. Not to mention the positive impact eSource will have on improving patients’ lives.
eSource goes way beyond electronic health records (EHR): it includes electronic clinical outcome assessment (eCOA), direct data capture (DDC) and eConsent.
Mike Novotny, founder and CEO of Medrio, Eunhee Chung, Director of Global Clinical Development at Souseikai Global Clinical Research Center, and Simone Knab, Data Enterprise Architect, Executive Team at Linear Clinical Research, will share how sites, sponsors and CROs can catapult themselves to success with eSource.
- Reduce on-site monitoring visits by 50% and eliminate Source Data Verification (SDV)
- Streamline the time from measurement to data entry in Electronic Data Capture (EDC) from 8 days to nearly instantaneous
- Increase bandwidth to focus on recruitment and subject visits
- Real-time, more accurate data enables improved decision-making and patient safety
- Increase study capacity and greatly reduce Clinical Research Associate (CRA) burnout
Get ahead of your competition by using eSource solutions with this free webinar. Join us by registering today.
Who Will Benefit
- Clinical Operations
- Site Coordinators
- Clinical Research Associates
- Principal Investigators
- Data Managers
Meet Your Presenters:
Mike Novotny is the Chief Executive Officer of Medrio, which he founded in 2005 in San Franciscso. Mr. Novotny applies 25 years of experience in research and software to his eClinical SaaS vision. Prior to founding Medrio, he was president of Ninaza, an EDC software company. He had previously held roles as a research associate at the United Nations and a manager of the fraud database at VISA.
Dr. Chung is the Director of Global Clinical Development at SOUSEIKAI Global Clinical Research Center in Japan. Dr. Chung plays a key role in advisory and consulting roles for early clinical trial safety. She heads the Global Development team in promoting and maintaining top-notch global-standard early clinical studies at SOUSEIKAI. Dr. Chung has a Master’s in Neuropharmacology and a Ph.D. in Neuropharmacology and Neuroscience.
Simone Knab is the Enterprise Data Architect at Linear Clinical Research in Perth Western Australia. She has 14 years experience working with and validating Clinical EDC platforms and databases. She’s led extensive, first-time eSource development, validation, and training for top 5 Pharma organizations and large investigator sites Ms. Knab was responsible for implementing eSource (Medrio DDC, ePRO and EDC) at Linear Clinical Research which is up to their 64th study using Medrio eSource since implementation.