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.

Beginner’s Guide to Pre-IND Meetings

New to the process of helping to bring a drug to market? As intimidating as…

Read More

Clinical Trial Associates and the Future of Pharma

Now more than ever, there is enormous pressure to deliver products to the market faster…

Read More

What do I do About Incidental Findings in Research?

An incidental finding is a “finding” or result from an intervention or test that uncovers…

Read More

What Goes into a Charter for DSMB or Endpoint Adjudication?

Learn the essentials of creating a robust charter for DMCs and EACs—an indispensable tool for…

Read More

5 Considerations for Evaluating an eIRB System

In addition to other responsibilities, human subjects protection programs (HRPPs) and IRBs are tasked with…

Read More

The Powerful Potential of Open Collaboration

Advarra’s Site-Sponsor Consortium emphasizes shared standards and transparent dialogue, paving the way for scalable, collaborative…

Read More
Onsemble Conference photo

Reuniting and Reconnecting at the 2022 Onsemble Conference

Throughout the day on Tuesday, March 29, clinical research professionals arrived at the Westin Savannah…

Read More
A decorative image for Regulatory Considerations Document for mRNA Research

mRNA Clinical Trials: Key Regulatory Considerations

Over the past two years, Operation Warp Speed brought mRNA-based vaccines into the spotlight, as…

Read More

Clinical Endpoint Adjudication Committees: Not Just for “Endpoints”

This blog outlines some of the critical events where endpoint adjudication committees (EACs) can be…

Read More

A Look at the Processes Behind Clinical Endpoint and Event Adjudication

See how Advarra’s tech-enabled adjudication platform leverages expert collaboration and secure data integration to streamline…

Read More

A Journey in Support of Diversity

Since he was young, Sergio Armani has always found solace on the bike, spending many…

Read More

The Impact of Digital Transformation in Clinical Trials

Digital transformation. We’ve heard about it for years, but now all of us have experienced…

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