3 Must-Haves to Deploy Remote Clinical Trials
This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities at your organization.
sites
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant experience, and overall study efficiency through technology integration.
Understanding Medical Science Liaisons and Clinical Liaisons
Research organizations utilize a variety of medical professionals to conduct successful clinical trials. Two of those positions are a medical
Maintaining a Robust Clinical Trial Pipeline
The clinical research landscape is likely forever altered by the COVID-19 pandemic, especially regarding trial continuity and the potential for
4 Key Integrations for Your Clinical Trial Management System
In this blog are some key CTMS integrations — using systems your institution has likely implemented — your team can use to streamline research operations.
Ideas for Managing Clinical Trial Finances Post-Pandemic
While the pandemic’s long-lasting effects on clinical trials are not yet fully known, effective financial management is a critical component
Key CTMS Capabilities to Improve Financial Management
A well-utilized CTMS streamlines financial workflows, automates participant payments, tracks budgets, and centralizes data, helping clinical sites maximize ROI and efficiency.
Why Institutions Should Consider an Externally Administered IBC
Clinical trials for gene therapy are booming, especially in the fields of oncology, infectious diseases, rare diseases, and regenerative medicine.
Site-Driven Metrics: Operational Data To Improve Research
The true value of metrics is to measure operational performance in order to improve internal processes. In clinical research, this is highly beneficial when applied where the work is conducted: at the sites.
Addressing Barriers to DEI in Clinical Research
Breaking down barriers to participation in clinical research has long been a challenge, affecting every aspect of the industry. As
Q&A from Remote Monitoring: Study Compliance In A Changing World
In a recent webinar, Advarra experts Emily Eldh and Ben Shankle provided insights and information in Remote Monitoring: Study Compliance
Regulatory Fine Points: What Research Sites Need to Do for Part 11 Compliance
To maintain Part 11 compliance, research sites must validate electronic systems storing FDA-regulated records, safeguarding data integrity and accuracy.