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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.
Impact of COVID-19 Outbreak on Ongoing Research and Protocols Under Advarra IRB Review
Advarra has policies and processes in place to keep IRB operations functioning as normal during the current coronavirus outbreak. The IRB continues hold 15 meetings a week and has been prioritizing the review of the numerous coronavirus protocols received as well as amendments relating to changes in research conduct because of unforeseen circumstances.
Effectively Working with a Research Technology Vendor During Implementation
Maintaining an effective partnership with your technology vendor is key to implementation success.
Biopoint Treatment Scheduler
The Biopoint Treatment Scheduler ensures that each of your OR rooms, treatment rooms, or other resources are filled to capacity.
Enhancing User Experience, Security, and Compliance with Single Sign-on
As technology evolves and the industry streamlines research workflows, implementing SSO can lead to significant improvements in both user experience and security.
Streamline Study Startup with Improved Site Selection & Feasibility
Identifying the best prepared and performing sites for a study is essential to success. Explore strategies to improve site selection and feasibility.
Q&A Part II: Clinical Trial Feasibility: Ensuring Success for Clinical Sites
Part 2 of Q&A from the Clinical Trial Feasibility: Ensuring Success for Clinical Sites webinar outlining why it is important for sites to approach research operations as a business.
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.
Regulatory Fine Points: What Research Sites Need to Do for Part 11 Compliance
Summary of James Riddle's Presentation at SQA, which outlines considerations for sponsors when ensuring 21 CFR Part 11 compliance at sites.
What Goes into a Charter for DSMB or Endpoint Adjudication?
This blog outlines the key elements of a DMC/EAC charter document, explaining its importance in conducting safe and compliant research.
Community Advocacy
Advarra is committed to sharing expertise with the research community to promote professional development, discussion, & collaboration
How Sponsors and Sites Work Together to Improve Protocol Compliance
As trials continue to increase in complexities, sites and sponsors must work together to minimize deviations and cause for FDA findings.
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