Clinical Leader Webinar

  1. A Real World Look At Leveraging Disruptive mHealth Technologies Increasing The Speed Of Research

    Learn how a current clinical study is leveraging disruptive mHealth technologies to ensure that collecting study data is accurate, seamless, and convenient.

  2. The last major frontier in automating clinical operations: Study Startup

    There has been a strong focus on study conduct, but as stakeholders are increasingly aware that better SSU processes are linked to shorter clinical timelines, the emphasis is shifting in that direction.

  3. Driving Informed Decisions In Site Selection: It's A Two-way Street

    The webinar will focus on study startup and discuss site selection practices from both the site and the Sponsor/CRO perspective.

  4. Innovations In E-Consent: Reducing Regulatory Risk While Improving Participant Comprehension

    Informed consent has a major impact on regulatory compliance, enrollment rates and expenses across the life of your study. Yet the traditional paper-based process has transformed informed consent into one of the most cited deficiencies.

  5. The Role of Transparency in CRO-Sponsor Partnerships: Enabling Better Collaboration Models

    This webinar will address common collaboration obstacles from both the CRO perspective and the sponsor perspective with a focus on increasing the value of strategic partnerships.

  6. eCOA Essentials: 1 Hour To Higher Quality Data

    The industry's shift from paper to electronic Clinical Outcome Assessments (eCOA) in clinical trials is happening at dizzying speeds.

  7. Innovative Mobile Technologies For Clinical Trials And CRA Monitoring

    Learn about mobile innovation for virtual, hybrid, and site-based clinical trials using the Clinical Reach™ mClinical™ platform for patient enrollment, engagement, and management on a global scale. Followed by an in-depth Q&A session and Parallel 6 Chief Medical Officer, Brad Pruitt, M.D., MBA, who demonstrates the newly released mobile data monitoring solution which is designed to empower clinical research associates (CRAs). 

  8. The Importance Of Engaging A Patient’s Support System During A Clinical Trial

    Learn how innovative mobile technology helps clinical trial participants stay engaged and compliant through the empowerment of the patient’s loved ones. Speaker, Stephen J. Freedland, M.D. (Urologist at Cedars Sinai DEPT of Surgery), presents a compelling case discussion on the importance of patient compliance and market approval, followed by Chief Medical Officer of Parallel 6, Brad Pruitt, M.D., MBA, who demonstrates the new Clinical Reach™ companion app followed by an in-depth Q&A session covering clinical use and various trial applications.

  9. eCOA And Equivalence Testing: New Evidence From Meta-Analysis

    The evaluation of the compatibility between scores from an electronic version of a paper-based questionnaire, better known as equivalence testing, is usually taken as a requirement for ensuring that data from electronic versions of patient reported outcomes does not vary from that captured on paper. This webinar discusses the results of a recently published meta-analysis which examined all published equivalence tests from 2007 to 2013. This webinar discusses equivalence testing, how the current meta-analysis run, and what the results mean in context of the field of eCOA.

  10. Using ePRO With Smart Devices

    Interest in using electronic patient reported outcomes (ePRO) on smart devices is on the rise. In this webinar, Emily Cantrell and Becky Baggett will share lessons learned working on a large phase 3 pain study that utilizes ePRO on tablet devices.