x

Join Advarra

Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

See Jobs

 
Blog

IRB Review of Coronavirus and Other Emerging Infectious Disease Research: Issues to Consider

Advarra IRB experts discuss unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review. Read more:

Read Now
5 min. read
Read more
 
Blog

Are “Virtual Trials” Mainstream Yet?

Advarra VP of Insitutional Services James Riddle discusses using virtual trial components in traditional study designs. Read more:

Read Now
5 min. read
Read more
 
Blog

Key Biosafety Considerations for Coronavirus Research

Advarra Director of Biosafety Daniel Eisenman reviews opportunities, risks, and risk mitigation strategies for coronavirus research. Read more:

Read Now
7 min. read
Read more
 
Blog

Revised Common Rule Compliance Now in Full Effect—and What That Means

The Revised Common Rule is here after multiple delays, exceptions, and many training sessions. As of January 20, 2020, this regulation is in full effect.

Read Now
3 min. read
Read more
 
Blog

Beyond the Regulations: More Considerations for Emergency Research

Go beyond the regulatory requirements and examine three key actions research organizations must consider before conducting planned emergency research.

Read Now
7 min. read
Read more
 
Blog

Most Popular Blogs of 2019

What did the research community enjoy most in 2019? Read Advarra's most popular blogs from industry experts and IRB members here.

Read Now
2 min. read
Read more
 
Blog

Reporting to the IRB: What NOT to Report

Reportable events can be tricky: according to the regulations, not every unanticipated event should be submitted to the IRB.

Read Now
6 min. read
Read more
 
Blog

Making Sense of the New HUD Guidance

Understand how the new HUD guidance clarifies responsibilites of the IRB and institutions, while widening the access of small communities to HUDs.

Read Now
7 min. read
Read more
 
Blog

Should Social Media Be Part of Your Research Toolbox?

Social media has emerged as a valuable tool for diverse stakeholders across the research community. Learn about the risks and benefits in this article.

Read Now
5 min. read
Read more
 
Blog

A Tale of Two Sites: The Power of Integrated Research Administration

Learn how institutions attract more studies from the the tale of two sites: one with an integrated research administration, and one without.

Read Now
5 min. read
Read more
 
Blog

Compensating Clinical Trial Participants: The Basics

Participant compensation is often a complicated matter. This blog will shed light on what an IRB considers during its review.

Read Now
5 min. read
Read more
 
Blog

What Is a Screening Consent?

Study-specific screening consent is a subtype of informed consent, which ensures a research participant understands of the research and its risks.

Read Now
3 min. read
Read more