Research Operations
Clinical Trial Feasibility: Ensuring Success for Clinical Sites
With comprehensive research portfolios and a myriad of operational challenges to manage, it has never been more important for sites to approach research operations as a business.
GCP Assessment During COVID – “Did Your Clinical Trials Remain GCP Compliant During COVID-19?”
Almost a year into the COVID-19 pandemic, analyze how IRB submissions, informed consent, and remote monitoring practices have maintained GCP compliance.
10 Things Site Staff Told Us
Site staff are the operational hands and feet of your clinical study, and much of your success relies on their success.
Above & Beyond: Better Utilize In-House Reporting Resources with Advarra Insights
Does your organization utilize your in-house reporting teams and systems to their full potential? Learn how a standardized business intelligence system could complement your current reporting structure to improve your organization’s operations.
4 Reasons Your Institution Needs an eRegulatory System
Using physical binders or an internal shared drive can slow research operations. Implementing an eRegulatory system helps institutions streamline research by transforming key workflows.
How Sites Can Win in the New Age of Genetically Engineered Treatments
The accelerating gene therapy market is expected to grow 16.6 percent by 2027. As gene therapies enter the pipeline, how can sites prepare themselves to take advantage of the rush?
The Power of Getting Everyone in Your Clinical Trial to Work as One Team
Everyone wins when all the stakeholders of a trial work together as a team. Yet, providing this sense of camaraderie across the study ecosystem is difficult.
How Staff Augmentation Assists with Successful Data Migration
With the goal to move active data from one system into OnCore CTMS, Advarra’s Staff Augmentation team worked with a customer’s associated hospital as it was faced with software termination.