Articles, App Notes, Case Studies, & White Papers

1. Unlocking New Clinical Insights With Remote Captured Sleep Data 3/25/2022

   Physicians, researchers, and drug developers need better data on sleep but capturing rich, real-world data in formal clinical trials has been difficult. Gain insight into ways to start collecting quality sleep data remotely by leveraging cloud-based data ingestion and processing.

    

2. Gradually Investing In Direct Data Capture Is Inevitable 2/2/2023

   Given study decentralization and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”

3. SMART On FHIR: Auto-Populate eCRFs On Study Day 1 7/10/2023

   Get an overview of SMART on Fast Healthcare Interoperability (FHIR) for clinical trials, including workflow improvements, real-world data (RWD) integration, and reducing researcher burnout.

4. The False Economy Of Paper Diaries In Clinical Trials 8/22/2022

   While paper diaries may appear cheaper, but there are hidden costs that make a digital eCOA solution much more affordable in your clinical trial.

5. Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC 2/23/2023

   Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.

6. Considerations For Implementing The Best eCOAs In Your Trial Design 5/2/2022

   Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.

7. eTMF Systems Tell Compelling Story Of COVID-19 Vaccines 3/7/2022

   The rapid development of Covid-19 vaccines may lead more drug developers to increase their speed and agility by adopting electronic Trial Master File (eTMF) systems. In the case of Covid-19 vaccines, discover how eTMF systems tell a dramatic tale.

8. Managing Clinical Trial Changes And Mid-Study Data Migrations 11/15/2023

   Explore how the Imperial College London was able to complete a successful migration of 14 ongoing studies, involving over 1,700 patients and 150,000+ forms, within a 16-month timeframe.

9. Automation Solutions For Safety Document Distribution 5/27/2022

   Discover how a leading global pharmaceutical company solved the problem of managed the distribution of safety reports by their clinical operations team.

10. Simplifying The Regulatory Submission Process With A Modern CTMS 12/14/2022

    Working in collaboration with industry representatives, explore the value that pulling the regulatory submission process into a modern Clinical Trial Management System (CTMS) could have.