E-Technologies STREAM

  1. Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies 4/30/2021

    Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure your TMF stays secure while remaining accessible to audits and inspectors so you can focus on getting your drug to market and not on finding documents. 

  2. ConneX - Expert Travel Solution For Clinical Trial Participants 5/3/2019

    ConneX is the most comprehensive clinical trial travel solution designed to meet the unique needs of your global trials.  

  3. Customer Testimonial – From CRA To Management 6/26/2024

    Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.

  4. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

    Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

  5. Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies 3/30/2023

    The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.

  6. Medable Total Consent: The Future Of Informed Consent 2/14/2023

    With Total Consent, Medable is transforming the consenting process – harmonizing it into one simple-to-use platform that enables trial sponsors and CROs to completely customize eConsent.

  7. Digital Versus Digitized: Common Misconceptions About eConsent 7/27/2022

    In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.

  8. IQVIA eCOA: Amplifying The Patient's Voice 4/19/2024

    Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.

  9. Unleash The Power Of IQVIA Complete Consent 11/12/2024

    Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.

  10. Smarter Trials Begin And End With Greenphire 2/10/2021

    Today’s clinical trials are more complicated and demanding than ever before. They’re often global, costly and require cumbersome travel. Greenphire is changing that. With our solutions, you can manage the entire financial lifecycle for trials conducted all over the world. Greenphire works directly with leading research institutions, sites, sponsors and CROs to simplify clinical trials and facilitate stronger, more collaborative relationships. With solutions that streamline your workflows, you can focus on providing better patient care.