Short form consents provide a crucial bridge for unexpected non-English speaking participants, ensuring informed consent remains accessible when translations aren’t readily available.
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
Advarra expert Steffen Engel answers questions from the recent webinar, Stepwise Implementation of a Clinical Quality Management System. Q: How
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
