Sites

Sickle cell disease significantly impacts the African American population, a minority community historically underserved by clinical research.

Optimizing Your Data Management Plan: Best Practices for Biomedical Research under the NIH Data Sharing Policy

Measuring IRB quality is often an effort to determine whether an IRB’s actions improve research participant protections.

Medicare coverage analysis evaluates how clinical research protocol items and services are billed per federal agency guidelines.

As the industry continues to shift from brick-and-mortar trials to more convenient hybrid formats, eConsent proves to be useful.

A valuable tool for both sites and participants, now is the right time for sites to adopt an eConsent platform.

Proper trial financing ensures internal costs are covered, facilitates better negotiation, and leads to higher compliance in trials.