Q&A – Regulatory Fine Points: Exploring 21 CFR Part 11 Validation
In a recent webinar, James Riddle, Shannon Roznoski, and Stuart Cotter of Advarra presented Regulatory Fine Points: Exploring 21 CFR Part
In a recent webinar, James Riddle, Shannon Roznoski, and Stuart Cotter of Advarra presented Regulatory Fine Points: Exploring 21 CFR Part
The processes necessary to support regulatory compliance require valuable time and resources within a clinical research institution. Regulatory tasks in particular require frequent
Learn how Inova Health System achieved a 20% increase in regulatory efficiency through Advarra eReg, optimizing operations without extra staff.
It’s safe to say 2020 has been more unpredictable than anyone could imagine. Through these unprecedented times, we have worked to provide the
Top 20 Biopharma Doubles Recruitment and Reduces Screen Failures Across 188 Sites A top-20 pharmaceutical company conducted a complex Phase
FDA has recently issued guidance relating to changes for Certificates of Confidentiality (CoCs) brought about by the 21st Century Cures
On-demand eLearning maximizes ROI by cutting classroom costs and offering accessible, effective training that aligns with modern clinical research needs.
In this case study learn how Advarra Study Startup and Advarra Enroll helped a top-30 pharmaceutical company achieve study startup milestones on time while setting their sites up for recruitment success.
The data gathered in a clinical trial is often collected by many different people, including investigators and coordinators, and interpreted
Discover how CU Anschutz and Novant Health leveraged OnCore technology to overcome pandemic challenges and achieve significant ROI in research.
We are honored to support a resilient research community during the COVID-19 pandemic. See the data points in our infographic to find out how Advarra helps keep research moving forward.
Edit checks are a great mechanism to improve data quality within an electronic data capture (EDC) system. There are many