Blog

Most training programs are outdated, unengaging, & redundant. Learn how to make a program achieving both regulatory requirements & your goals

In this blog, we share tips and best practices for writing an impactful clinical audit report.

By utilizing a vendor that offers both IRB and IBC services in-house, sponsors can streamline reviews and enhance study startup timelines.

Virtual, remote, hybrid, decentralized, mHealth, telehealth: Find out what these terms mean for clinical research.

Faced with expanding their budgets, sponsors and sites must enable budgeting and billing compliance best practices starting at study activation.

Partnering with Advarra, one nonprofit successfully obtained an Emergency Use Authorization from the FDA within five weeks.

Emergency preparedness plans help institutions plan, prepare for, and respond to emergencies as they arise.

Explore the benefits of switching from paper to eSource, tips for implementation, and how to maintain compliance.

There is an increasing challenge to find eligible patients and build trial awareness, so how should the industry address them?

An Advarra expert provides insight in this Q&A session on the FDA inspection readiness process, including how to improve current workflows.

In this blog, we take a look at popular blog posts and webinars in 2021 garnering the most interest from research community members like you.

Advarra experts Joan Versaggi and Leslie Paul answer questions from the webinar- FDA Updates: BIMO – What Sponsors Need to Know.