Blog

Q&A from the Institutional Responsibilities Under a Federalwide Assurance (FWA) webinar and an overview of the FWA and its changes with the revised Common Rule.

There are many distinctions that set Phase I trials apart from the rest. For sites aiming for a successful Phase I trial, working with an organization that understands the nuances is key.

Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.

Learn how key eRegulatory integrations like email, local and central IRBs, and Clinical Trial Management Systems can accelerate study start up, increase compliance, and improve regulatory workflows.

Messenger RNA (mRNA) has made recent headlines due to its role in Operation Warp Speed. This article explores how its technology is used to fight the COVID-19 pandemic.

Elevating our consulting capabilities to accelerate clinical research and bring therapies to market sooner.

Fiction often shows warp speed travels not going as planned, but what does warp speed mean for vaccine development in clinical research?

We strive to create meaningful and relevant content for the clinical research community. Check out our top resources of 2020.

Certificates of Confidentiality protect participant privacy by preventing disclosed sensitive information during research.

Learn how to launch an eLearning program for Clinical Research. eLearning is a tool for software implementations, staff development, and procedure training.

Community-based participatory research (CBPR) is utilized to reduce racial and ethnic health disparities in under-represented populations.

Learn more about the importance of medical coding dictionaries, their common uses, and best practices.