Since joining forces a year ago, Advarra and Forte have worked to ensure altogether better research, integrating Advarra’s CIRBI platform and Forte eReg.
Recent regulations and policies have ushered in the era of mandated single IRB (sIRB) review. Many institutions must now establish policies and processes for working with an external sIRB.
Among the many challenges clinical research institutions are facing during the COVID-19 pandemic is the need to quickly adapt to remote workflows. We’re collaborating with leaders at academic research centers to address these issues and create new efficiencies in the post-COVID-19 research landscape.
In this Q&A, Dr. Luke Gelinas answers attendee questions from his webinar “Evaluating Payment to Participate in Research: Ethical and Regulatory Issues.”
There are unique issues that research involving emerging infectious diseases like coronavirus can raise for IRB review and research informed consent.
Choosing the right CTMS can enhance your billing compliance and minimize risk.
Collaboration, Education and Fun in the Sun: Why You Should Attend the 2020 Spring Onsemble Conference
Our Spring 2020 Onsemble Conference is right around the corner, and nearly all of our sessions will qualify for continuing education units.
Virtual trials have grown in popularity and usage over the last decade. Explore what that means for traditional sites and their future in the clinical research landscape.
Implementing and integrating a CTMS can be beneficial for your organization. Streamline your research operations with these 4 integrations.
Effective budget negotiation is consistently a hot topic for clinical research sites. Here are a few tips to make sure your site gets the most from your negotiations.