Patient Engagement Suite

  1. The Case For Patient Diversity In Clinical Trials 2/25/2021

    Uncover how a global pharmaceutical company met the FDA's challenge to increase patient diversity with a multi-tiered approach combining key tactics and technology.

  2. Pharma Sponsor Enlists Cenduit IRT To Rescue A Multi-Country, Multi-Site Oncology Study 2/24/2021

    After go-live, the sponsor learned its study did not fit the existing IRT solution, affecting data quality, timelines, and drug supply shipments. The legacy system’s medication management algorithm could not support the required flexibility in the supply chain. The trial included an adaptive cohort design. Read how Cenduit delivered a high-quality study achieved through innovation, close client collaboration, and expert project management.

  3. Flexible IRT Platform Solution For National Lung Cancer Trial 2/24/2021

    Trial design for a medicine trial to investigate treatment for non-small cell lung cancer presents unique challenges. These include the need for an IRT platform that can support the rapid incorporation of amendments and account for multiple or potential arms requiring different lists of material types and dosages that could be prescribed to patients and supplied to sites. Cenduit’s highly-configurable, flexible technology platform was the solution.

  4. Navigating Patient Consent Scenarios In COVID-19 Trials 5/20/2020

    Many people have questions on the topic of remote consent in a hospital setting, particularly when the patient is quite ill and requires a legally acceptable representative (LAR) to consent on his or her behalf. This article shares insights gained through real-world implementations of remote consent.

  5. Five Frequently Asked Questions (And Answers) About eConsent During The COVID-19 Crisis 4/17/2020

    For the clinical research industry, COVID-19 poses immediate and long-term challenges that require sharing experiences with the industry now more than ever. This article provides the most frequently asked questions about eConsent technology.

     
  6. Improving Supply Chain: Accountability, Sustainability, Optimization

    Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.

  7. Harness The Power Of eCOA In Your Next Trial

    In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.

  8. Patient Data: The Backbone Of Your Clinical Trial

    In clinical trials, data capture is typically centered around patients’ experiences with a drug. See why electronic clinical outcome assessments (eCOAs) are essential to patient data capture.