The Regulatory Binder Checklist For Clinical Trial Sites
A regulatory binder is essential for managing clinical trial documents, ensuring regulatory compliance, and facilitating audits. It organizes critical documents;
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eReg Benefits for Clinical Research: Use Cases for all Types of Sites
While regulatory management takes time and effort, using an eRegulatory system can help staff boost productivity, improve compliance, and save resources.
The ROI of eRegulatory and eIRB Integration
Integrating eRegulatory and eIRB systems streamlines document management, enhances compliance, and delivers significant ROI through time and cost savings per protocol.
Addressing Research Technology Challenges to Gain Sponsor Buy-in
At Advarra, we are passionate about enabling the industry to become more site-centric. To achieve this, it is especially important
eClinical Regulatory Trends Impacting Clinical Research
For the past two years, the clinical research industry has seen an acceleration in staff shifting to a remote, work
Ensuring a Successful and Collaborative SDLC Process
At Advarra, it’s our mission to ensure safer, smarter, faster clinical research every step of the way in the research
How to Be Research Ready: Today and Beyond
Research readiness ensures that your organization can accept, activate, and adapt to new studies and opportunities no matter the regulatory circumstances.
Building a Foundation for Regulatory Success in the Post-Pandemic Landscape
The past year has been one of the most challenging ever for those working in healthcare and clinical research. The
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.
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.