Research Operations
Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)
Learn how to ensure compliance with FDA 21 CFR 312.32, and explore Advarra solutions that support efficient and compliant safety reporting.
Study Activation: Top Four Takeaways from Research Sites
How can sponsors leverage their relationship with their sites to ensure more efficient research?
Site-Driven Metrics: Operational Data To Improve Research
Most metrics are geared toward sponsors and CROs, find out how this ultimately impacts site research operations
Virtual Investigator Meetings
Advarra’s Virtual Investigator Meetings expedite site activation and increase investigator attendance, comprehension, and engagement.
Vendor Management and Oversight of Clinical Trials
This white paper provides practical insights and guidance on the key concepts that will help any sponsor better manage their clinical trials.
Study Activation Survey Results and What it Means for Sites
In this episode, we review results from Advarra's recent survey and discuss study activation success strategies for sites.
How to Successfully Conduct Virtual Investigator Meetings
Explore best practices to conduct virtual investigator meetings to increase comprehension and expedite site activation.
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.
Cell & Gene Therapy vs Drug Research: What’s the Difference?
In the past year, cell and gene therapy research has exploded. Understand how this field differs from traditional drug development.
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?
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