On-Demand Webinar

Making Mobile Clinical Trials a Reality

New technologies and related methodologies could offer clinical research professionals expanded capacity for low-cost, efficient, and expansive collection of high-quality participant data—both within and beyond the clinical setting.

The Clinical Trials Transformation Initiative’s (CTTI’s) Mobile Clinical Trials (MCT) program seeks to create strategies and solutions related to incorporating these new tools. Ultimately, adoption of this program’s recommendations and tools could also facilitate patient recruitment for clinical trials, improve participant experience, and result in reduced loss to follow-up.

In this webinar hosted by Advarra, presenters will share findings, recommendations, and resources from 4 projects in CTTI’s MCT program: Novel Endpoints, Mobile Technologies, Decentralized Trials, and Stakeholder Perceptions.

Learning Objectives

Following this free webinar, attendees will be able to:
  • Define ways to build technology into study planning and conduct
  • Identify practical considerations for sites utilizing mobile technologies
  • Recognize IRB/ethics considerations regarding mobile clinical trials

Presented By

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Michele Russell-Einhorn


Chief Compliance Officer and Institutional Official

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Greg Licholai


Chief Medical Officer and Faculty
PRA Health and Yale School of Management

Who Should Watch?

The content of this webinar applies to investigators, study staff, IRB representatives, and others involved in developing and implementing mobile technologies in clinical trials.

CEU Credits

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations. 

This session meets the Certified IRB Professional (CIP) recertification guidelines for a maximum of 1 credit. 

The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.

If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.

Certificate of Attendance

After completing this webinar in its entirety, you will receive a certificate of attendance. This certificate will include your full name, and it will be emailed to you at the end of the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and take the survey at the end. Visit our Webinar Help page for more information on certificates of attendance.

Duration: 1 hour

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