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Gene Therapy Ready Site Network
This info sheet describes Advarra’s Gene Therapy Ready site network and the benefits of joining the network.
Effective Clinical Trial Financial Management Post-Pandemic
This eBook investigates shifting fiscal priorities and strategizes how sites can ensure effective financial management post-pandemic.
IRB Services for Institutional Sites
Advarra serves as your external support and compliance partner for everything from single investigational sites to multisite research consortia and therapeutic networks.
When do I Need a DMC?
View our infographic to learn the basics of a data monitoring committee (DMC), also referred to as data safety monitoring board (DSMB).
Advarra IRB Chairperson Featured in PRIM&R Blog About Patient Centered Outcome Research
Advarra IRB Chairperson Luke Gelinas was recently featured in the PRIM&R blog post Recommendations for Oversight of Patient-Centered Outcomes Research
Inventory, Quality Control and Scanning of Trial Master Files
Advarra Consulting assists a small specialty biopharmaceutical company in upgrading storage of TMFs to a comprehensive electronic filing system.
General Perceptions of Clinical Trials in 2023
In order to gauge the general perception and understanding of clinical research, we conducted a poll on awareness & participation in trials.
Engagement in Research for Pragmatic Clinical Trials
Judith Carrithers contributed to the article Engagement in Research for Pragmatic Clinical Trials for the NIH Health Care Systems Research Collaboratory.
For-Cause Investigation of Potential Misconduct and/or Fraud at Two of Site Management Organization’s Locations
Advarra Consulting helped a site management organization pinpoint and correct suspected fraud at two study sites. Read more about Advarra’s investigation into the misconduct in this case study.
Advarra Biosafety Director Contributes to Lab Manager Magazine
Advarra Director of Biosafety Services Dan Eisenman recently contributed to an article in Lab Manager Magazine
Evaluation of Clinical Systems Requirements
Advarra Consulting assesses a mid-size device company's processes, determining the need for new and modified electronic systems and processes and proposing a CTMS.
An IRB Perspective on Improving Informed Consent
Julie Blasingim co-authored the article An IRB Perspective on Improving Informed Consent in Clinical Researcher.
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