On-Demand Webinars

1. IRT And Direct-To-Patient Trials 1/12/2022

   Want to know more about the growth and expansion for IRT in the decentralized trial space? Witness how IRT is being used to support direct-to-patient delivery in this hybrid trial case study presentation. 

2. Proven Practices For ePRO Adoption 12/8/2022

   Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.

3. Agile eConsent: Taking A Flexible Approach To Global Implementation 6/28/2022

   Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.

4. Navigating The RWD Landscape In Japan 1/12/2023

   Take a deep dive into the current system and database utilized in Japan and delve into tips for database selection and how it should be selected according to target disease area and desired result.

5. Securing High-Quality Patient Referrals From HCPs...Faster! 10/13/2023

   Looking to minimize time on outreach or accelerate patient recruitment? Uncover how this partnership was able to deliver positive overall results for sponsors, ultimately benefiting patients.

6. RTSM Considerations For Master Protocol Oncology Studies 1/20/2022

   This webinar discusses the types of master protocols and how configurable, modern RTSM systems enable fast and seamless mid-study changes to help you efficiently run your master protocol study.

7. eConsent – The Enrollment Solution For Decentralized Trials 2/1/2022

   The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.

8. Right-Size Your eConsent Approach 11/17/2023

   Delve into the art of tailoring the eConsent experience to match the specific needs of your study and patients, such as how to craft patient-centric eConsent documents, select appropriate delivery models, and more.

9. 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.

10. Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF 4/17/2023

    Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.