Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

Advarra Blog

FEATURED Post

Ways to Streamline Informed Consent Process in Clinical Trial Startup

Optimizing the informed consent process is critical for accelerating clinical trial startup while maintaining compliance and participant understanding. This article explores key strategies for streamlining informed consent, including leveraging electronic consent (eConsent) solutions, standardizing templates, and improving collaboration between sponsors, sites, and IRBs. By implementing these best practices, research teams can enhance efficiency, reduce delays, and improve the participant experience in clinical trials.

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…

Read More

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…

Read More

Defining Decentralized Clinical Trials and Understanding Their Nuances

Decentralization is one arrow in the quiver to modernize clinical trials.[1] Yet, owing to the…

Read More

To Be Patient-centric, Be Site-centric

Patient centricity has long been a key goal in healthcare, as well as in clinical…

Read More

Digital Health, COVID-19, and the Evolution of Clinical Trials

  The COVID-19 pandemic has driven transformative changes across industries, and clinical research is no…

Read More

Legislation to Advance Equality and Inclusion in Oncology Clinical Trials

According to the Association for Clinical Oncology, individuals who identify as African American or Black…

Read More

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,…

Read More

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…

Read More

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…

Read More

FDA Inspection Readiness: After the Inspection

In the final part of the three-part FDA inspection readiness series, we will go into…

Read More

FDA Inspection Readiness: During an Inspection

In our previous blog, FDA Inspection Readiness: Preparing for an Inspection we reviewed how to…

Read More

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…

Read More

Looking for More?

To register for upcoming webinars and see where we’ll be next, go to the Events page.

Want to see the latest news and updates about Advarra? You can find them in the Newsroom.

Are You Ready To Bring People Together for Better, Faster Trial Outcomes?

Subscribe to our monthly email

Receive updates monthly about webinars for CEUs, white papers, podcasts, and more.

Scroll to Top