Technology
Site Technology Guide for Facilitating GCP in Decentralized Trials
Download the white paper to learn how to adhere to Good Clinical Practices (GCP) while managing the entire decentralized trial process.
Advarra eConsent
Simplify oversight and expand remote consenting capabilities with Advarra’s 21 CFR Part 11 compliant electronic consent management system.
Succeed in the New Research Landscape with Site Training Technology
In this webinar, we evaluate critical requirements and advanced workflows life sciences companies should look for in site training technology.
Addressing Barriers to DEI in Clinical Research
A diverse, equitable, & inclusive research environment benefits everyone: trials & the communities alike. How can sites incorporate more DEI?
Making the Most of Site Training: Lessons from the Pandemic
Ensure that your next remote site initiation visit is both productive and useful despite the virtual setting with these tips
The Power Of Patient Advocacy In Drug Development
This blog outlines the origins and rise of patient advocacy groups, discussing the milestones in the FDA's acceptance of these groups.
Q&A from Remote Monitoring: Study Compliance In A Changing World
In a recent webinar, Advarra experts provided insights and information in Remote Monitoring: Study Compliance in a Changing World
Improving Access to Research for Diverse and Underserved Populations
Increasing diversity and inclusion in research has long been a challenge in the clinical research community. Learn strategies to increase access to clinical trials for all.
Industry-Wide Solutions to Improve Access to Clinical Trials
In this discussion, panelists provide actionable strategies for improving access to clinical research for diverse, underserved populations.
How to Be Research Ready: Today and Beyond
If presented with a new study, are you prepared to take it on? Efficient study activation can set the pace for a successful clinical trial.
Building a Foundation for Regulatory Success in the Post-Pandemic Landscape
Read how an eRegulatory system can increase productivity, improve compliance, and ensure a return on your technology investment.
Q&A: FDA Inspections of Clinical Investigators: Understanding the Process and What to Expect
Q&A from our 4/21 webinar outlining what to expect in an FDA inspection and how to have a more positive experience.
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