Advarra
- 7 profiles
- 5 categories
All Profiles
Streamline Your Regulatory Process with eReg. Think beyond the binder. Save money, improve efficiency, and enhance regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory workflows for any size research site.
OnCore is more: its not just a system; its a collaborative community that advances clinical research operations.
A CTMS designed to accommodate the unique needs of your organization. Revolutionize the way you conduct your clinical research.
Forte EDC supports leading academic research centers, cancer centers, and health systems in running successful and compliant IITs.
Advarra Connect® process replaces manual, error-prone processes with technology that automates the secure transfer of IRB-related documents directly from the Advarra® CIRBI Platform to your electronic trial master file (eTMF) without manual loading or manipulation of documents before export.
One platform that centralizes and simplifies IRB management
Advarra Reviews
Michelle W.
Clinical Trial Budget AnalystCalendars and Financials
Geneva M.
Data Scientist in Healthcare ResearchI haven't used it very much yet, but so far so good
Matthew R.
Advarra eReg--Pretty good, but could be better
About
What is Advarra?
Advarra is a leading clinical research organization (CRO) specializing in providing comprehensive services for clinical trials across various therapeutic areas. With a focus on advancing medical research, Advarra offers expertise in study design, patient recruitment, and regulatory compliance. The organization is dedicated to supporting pharmaceutical, biotechnology, and medical device companies in bringing innovative treatments to market. Their commitment to quality and efficiency is reflected in their extensive experience and robust network of research sites. For more information, visit their website at [advarra.com](https://www.advarra.com/).
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