Blog

Infection Control and Biosafety in Gene Therapy Research

Given the growth in gene therapy research, sponsors, CROs and sites have become increasingly curious about the requirements to be able to conduct such studies.

Read Now
4 min. read
Read more
 
Blog

Integration Update: Leading Compliance Adherence

The Advarra team is proud to announce that all major integration activities are now complete.

Read Now
3 min. read
Read more
 
Blog

Test Your Knowledge: Clinical Research Acronyms Quiz

Whether you are new to the industry or a seasoned professional, test your knowledge on common clinical research acronyms.

Read Now
1 min. read
Read more
 
Blog

ICH-GCP Guidelines and Research Conducted in the US

Learn the basics of how ICH-GCP Guidelines can impact the study ICF and how we at Advarra came to our updated policy on the topic.

Read Now
3 min. read
Read more
 
Blog

What’s the Difference Between Right to Try and Expanded Access?

Let’s take a look at the basics of what each program does and does not do for patients seeking to access investigational therapies.

Read Now
5 min. read
Read more
 
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