A Checklist for Optimizing Clinical Trial Study Startup Activities
From protocol design to site training, optimizing study startup requires meticulous planning and collaboration to ensure timely trial activation.
From protocol design to site training, optimizing study startup requires meticulous planning and collaboration to ensure timely trial activation.
Pre-screening subjects is common practice at most sites. In this article, learn some best practices and how technology can play an important role.
Like every institutional review board (IRB) – commercial or local – Advarra is subject to inspections from time to time.
Optimizing clinical trial access for potential patients is a critical goal for researchers and sponsors. How can we make clinical
Integrating eRegulatory and eIRB systems streamlines document management, enhances compliance, and delivers significant ROI through time and cost savings per protocol.
An incidental finding is a “finding” or result from an intervention or test that uncovers a condition or problem that
In addition to other responsibilities, human subjects protection programs (HRPPs) and IRBs are tasked with ensuring a research protocol’s lifecycle
Throughout the day on Tuesday, March 29, clinical research professionals arrived at the Westin Savannah Harbor Golf Resort & Spa
Over the past two years, Operation Warp Speed brought mRNA-based vaccines into the spotlight, as organizations like Moderna and Pfizer/BioNTech
Since he was young, Sergio Armani has always found solace on the bike, spending many childhood days riding 20 miles
At Advarra, we are passionate about enabling the industry to become more site-centric. To achieve this, it is especially important
Understanding clinical trial billing rules, from Medicare policies to state laws, is crucial for avoiding compliance pitfalls and supporting trial integrity.