4 Questions to Ask CTMS Vendors
Here are four questions to ask during the CTMS selection process to offer more insight into your future success with the selected vendor.
Here are four questions to ask during the CTMS selection process to offer more insight into your future success with the selected vendor.
Phase I research demands careful IRB oversight, balancing participant safety with timely reviews. Proactive strategies can help address its unique challenges.
This blog covers three must-have decentralized trial tools to efficiently and compliantly implement remote modalities at your organization.
eSource, ePRO, and EDC each play distinct roles in clinical trials, enhancing data consistency, participant experience, and overall study efficiency through technology integration.
Research organizations utilize a variety of medical professionals to conduct successful clinical trials. Two of those positions are a medical
The clinical research landscape is likely forever altered by the COVID-19 pandemic, especially regarding trial continuity and the potential for
In this blog are some key CTMS integrations — using systems your institution has likely implemented — your team can use to streamline research operations.
While the pandemic’s long-lasting effects on clinical trials are not yet fully known, effective financial management is a critical component
A well-utilized CTMS streamlines financial workflows, automates participant payments, tracks budgets, and centralizes data, helping clinical sites maximize ROI and efficiency.
Clinical trials for gene therapy are booming, especially in the fields of oncology, infectious diseases, rare diseases, and regenerative medicine.
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.
Breaking down barriers to participation in clinical research has long been a challenge, affecting every aspect of the industry. As