IRB
Beyond Pharmaceuticals: Research Involving Cosmetics, Conventional Foods, and Dietary Supplements
Explore regulatory frameworks applicable to research involving cosmetics, conventional foods, and dietary supplements.
IRB Review of Decentralized Trial Technology
Explore the current regulatory landscape governing mHealth and virtual trial applications in clinical research.
AI in Clinical Research
In this episode, we explore the ethics and implications of artificial intelligence in clinical research.
Becoming Your Own Best Advocate Through Patient Empowerment
In this episode, we discuss clinical trial patient empowerment and advocacy. We dive into health literacy and the informed consent process.
IRB Services for Federal Grants
View this info sheet to learn about Advarra’s IRB expert oversight and guidance to support your next federal grant proposal.
Beginner’s Guide to Institutional Review Boards (IRBs)
In the U.S., there is an independent group overseeing clinical research, ensuring participants’ rights and welfare are protected.
What Level of Review Does Your Study Need?
In this infographic, we share useful information for investigators to know which level of IRB review likely applies to their study.
Reporting to the IRB: What Does and Does Not Need to be Reported
This white paper outlines IRB reporting requirements, why reporting is important, and what should and should not be reported.
James Riddle and Willie Muehlhausen Discuss Digital Technology and Virtual Data Collection in Clinical Research
In this episode, we discuss the growth of decentralized clinical trial technology and how IRBs evolved to account for technology advancements.
Study Startup Support Info Sheet
Advarra provides flexible solutions that help accelerate the initial IRB review process and make it more efficient.
Navigating the Ethics of Remote Research Data Collection
In this article, Luke Gelinas develops a framework to identify and address key challenges for remote research data collection.
US Medical Device Regulation 101
Speed the review process by understanding how medical devices are classified & what the IRB must review to approve device research.
Subscribe to our monthly email
Receive updates monthly about webinars for CEUs, white papers, podcasts, and more.
Advancing Clinical Research: Safer, Smarter, Faster™
Copyright © 2024 Advarra. All Rights Reserved.