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World’s Largest CRO Leverages Partnership With Integrated Central IBC to Initiate Sites in COVID-19 Vaccine Research at Warp Speed
Advarra’s IRB and IBC reviews and Gene Therapy Ready site network helped reduce study startup timelines and delivered trial results to the sponsor quicker than expected.
Virtual Investigator Meetings
Advarra’s Virtual Investigator Meetings expedite site activation and increase investigator attendance, comprehension, and engagement.
Transforming Your Research Administration Structure to Attract Research Opportunities
Institutions, health systems, and academic medical centers can dramatically increase their profile in the research community and attract major studies that move medical science forward on a global scale.
Data Monitoring Committee Info Sheet
Designing your data monitoring committee to provide the appropriate oversight to support participant safety and statistical evaluations.
Good Manufacturing Practices: When Do They Apply?
Ensure product quality and compliance in the drug development process. Learn how to optimize your manufacturing processes and maintain key regulatory standards with cGMP best practices from experts.
Accelerating the Recovery – Design and IRB Review of Safety Monitoring Plans During COVID-19
COVID-19 is rapidly changing the way research is conducted, namely how to conduct effective participant safety monitoring at a distance. Read more:
Can Ethics Review Catch Up to the CBD Craze?
CBD, a non-psychoactive cannabinoid, is experiencing a massive surge in popularity, but clinical research lags behind in verifying effective uses.
Why Institutions Should Consider an Externally Administered IBC
Gene therapy clinical trials require specialized oversight & expertise. Read how institutions can prep for the boom in gene therapy research.
Developing a Clinical Trial Budget Following Medicare’s Clinical Trial Policy and Device Regulations
Learn tips for developing and negotiating a clinical trial budget according to Medicare’s rules and regulations for device and drug clinical trials.
Managing Conflicts of Interest in Clinical Research
Managing conflicts of interest in clinical research is a critical mission for many reasons. Here we discuss the need for conflict of interest policies in clinical research, examine the specific role of an IRB in managing conflicts of interest, and review key elements that an IRB’s conflict of interest policy should include.
Clinical Research Nursing Core Curriculum
Candi Barlow of Advarra authored Chapter 8 on Recruitment and Retention in "Clinical Research Nursing Core Curriculum".
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