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.

Read Now
Resource
Info Sheets
Reset
Blog

Q&A Part II: Clinical Trial Feasibility: Ensuring Success for Clinical Sites

In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building…

Read More
Blog

Q&A Part I: Clinical Trial Feasibility: Ensuring Success for Clinical Sites

In a recent webinar, Advarra experts Wendy Tate and Cheryl Byers provided considerations for building…

Read More
Blog

The Impact of Public Perception of Clinical Research

Undoubtedly one of the biggest news stories around the world during the past year has…

Read More
Blog

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…

Read More
Blog

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
Blog

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
Blog

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
Blog

To Be Patient-centric, Be Site-centric

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

Read More
No Resource Type

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
Blog

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
Blog

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
Blog

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

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?

Sponsors
Sites
CROs

Subscribe to our monthly email

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

Subscribe
Scroll to Top