Q&A Part II with Dr. Wendy Tate, Author of Insights Accrual Prediction Algorithm
This week, Advarra launched a pilot of the Insights Accrual Prediction platform to customers, powered by Wendy’s initial model and […]
Research Operations
Q&A Part I with Dr. Wendy Tate, Author of Insights Accrual Prediction Algorithm
In every aspect of her research career, Dr. Wendy Tate, Director of Research Operations at Advarra, has been committed to
Insights Accrual Prediction Platform Leverages Machine Learning to Advance Better Research
While the clinical research industry has developed innovative therapies and devices to serve patients all over the world, the industry
Defining Decentralized Clinical Trials and Understanding Their Nuances
Decentralization is one arrow in the quiver to modernize clinical trials.[1] Yet, owing to the varied approaches and possible components
Building Remote Workflows within eRegulatory Document Management: Subject Binders & SOPs
Centralizing subject binders and SOPs in an eRegulatory system streamlines remote monitoring, ensuring secure access, compliance, and future-ready workflows.
How Technology Can Improve Regulatory Efficiencies During the COVID-19 Pandemic and Beyond
As we begin to emerge from the challenges of the COVID-19 pandemic, it’s clear that the post-pandemic landscape differs from
How Technology and System Integration Can Improve Your Billing Compliance
System integration streamlines clinical trial billing, ensuring accurate charge routing and reducing compliance risks through centralized workflows.
GCP Assessment During COVID – “Did Your Clinical Trials Remain GCP Compliant During COVID-19?”
We are now almost a year into the COVID-19 pandemic, and you may be asking whether your clinical trials remained
Above & Beyond: Better Utilize In-House Reporting Resources with Advarra Insights
With Advarra Insights’ core dashboards, research institutions streamline reporting, allowing custom teams to target institution-specific data needs.
4 Reasons Your Institution Needs an eRegulatory System
Finding new ways to more accurately and efficiently manage the regulatory compliance process is always a hot topic among researchers.
How Sites Can Win in the New Age of Genetically Engineered Treatments
With gene therapy trials on the rise, sites must prepare biosafety protocols, facility standards, and partnerships to attract cutting-edge studies.
How Staff Augmentation Assists with Successful Data Migration
Staff Augmentation aids data migration by assessing workflows, ensuring a smooth transition to OnCore, and empowering teams with tailored training.