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

The GDPR and Its Impact on the Clinical Research Community (Including Non-EU Researchers)

Please note that this material is provided for informational purposes only and not for the purpose of providing legal advice.

Read Now
7 min. read
Read more
 
Blog

Integration Update: Recent Milestones Completed

The Advarra team has worked to fully integrate our processes and policies to provide clients with unified capabilities and support for IRB, IBC and global research quality and compliance consulting services.

Read Now
4 min. read
Read more
 
Blog

Integration Update: Expanded FAQ for Advarra Merger Efforts

The following FAQ expands upon previous FAQs we’ve published and provides additional insight into the integration process.

Read Now
15 min. read
Read more
 
Blog

International Research and Research Ethics Review

Clinical research continues to grow throughout the world, with researchers looking outside the US for new and diverse subject populations to help develop and improve investigational therapies. Lauri Carlile, VP of Operations at Advarra, discusses the basics of ex-US research ethics review for US-based researchers.

Read Now
3 min. read
Read more
 
Blog

Clinical Research Acronyms and Abbreviations You Should Know

New to clinical research? Learn the meaning of common industry acronyms and abbreviations including eCRF, IIT, PI, TMF, and more.

Read Now
4 min. read
Read more
 
Blog

Integration Update: Revised FAQ for Advarra Merger Efforts

Since November 2017, the Advarra team (formerly Chesapeake IRB and Schulman IRB) has been working to integrate our process and policies. We are committed to being transparent throughout this integration, so we've assembled the following FAQ to keep you updated.

Read Now
8 min. read
Read more
 
Blog

Data Collection in Clinical Trials: 4 Steps for Creating an SOP

Learn the necessary steps to create an effective SOP for data collection in clinical trials when using an electronic data capture (EDC) system.

Read Now
6 min. read
Read more
 
Blog

Schulman IRB and Chesapeake IRB Merger and Integration: What You Need to Know

Chesapeake IRB and Schulman IRB are merging under the new organizational name, Advarra. This FAQ addresses commonly asked questions about this merger.

Read Now
4 min. read
Read more
 
Blog

Changes to NIH Policy for Issuing Certificates of Confidentiality: What You Need to Know

NIH’s policy for certificates of confidentiality changed so that CoCs are automatically issued for all NIH-funded research that uses sensitive information.

Read Now
4 min. read
Read more
 
Blog

Informed Consent in Research and Individuals with Impaired Decision-Making Capacity

This blog outlines the principle of equitable selection and the requirement for additional safeguards for certain vulnerable groups.

Read Now
4 min. read
Read more
 
Blog

Non-English Speaking Research Subjects: What’s in the Regs?

Recently, the clinical research community has been making efforts to include more diverse subject populations in clinical studies.

Read Now
4 min. read
Read more
 
Blog

Evaluating eConsent: Some Considerations from an IRB Perspective

eConsent technology can often better inform participants than just the traditional paper consent, which is great from an IRB perspective.

Read Now
5 min. read
Read more