Ideas for Managing Clinical Trial Finances Post-Pandemic
While the pandemic’s long-lasting effects on clinical trials are not yet fully known, effective...
FEATURED E-BOOK
Making Good Clinical Practice More Understandable
This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.
How to Design Digital Materials for Participant Engagement
Informative and engaging participant materials are an important part of any clinical trial, especially...
Building Patient-centricity in Clinical Trials: Lessons and Future Directions
The concept of patient centricity is a recurring theme in clinical research, but...
Key CTMS Capabilities to Improve Financial Management
A well-utilized CTMS streamlines financial workflows, automates participant payments, tracks budgets, and centralizes data,...
Why Institutions Should Consider an Externally Administered IBC
Clinical trials for gene therapy are booming, especially in the fields of oncology, infectious...
Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)
Read about IND safety reporting required under FDA 21 CFR 312.32(c), challenges faced in...
Study Activation: Top Four Takeaways from Research Sites
While enrolling subjects is arguably the most crucial aspect of clinical research operations, this...
Site-Driven Metrics: Operational Data To Improve Research
The true value of metrics is to measure operational performance in order to improve internal...
How to Successfully Conduct Virtual Investigator Meetings
In a remote clinical research landscape, a successful virtual investigator meeting can ensure a...
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