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.

Read Now
Resource
Info Sheets
Reset
Blog

How to Be Research Ready: Today and Beyond

Research readiness ensures that your organization can accept, activate, and adapt to new studies and…

Read More
Blog

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…

Read More
Blog

Q&A: FDA Inspections of Clinical Investigators: Understanding the Process and What to Expect

In a recent webinar, Advarra experts Constance Cullity and Michele Russell-Einhorn presented FDA Inspections of…

Read More
Blog

Phase I Oncology Clinical Trials

In a recent blog, we described the complexity and uniqueness of Phase I clinical trials,…

Read More
Blog

Study Startup Success for BioPharma and MedTech: Engage a Research Compliance Partner

A key element to successful study startup is identifying efficiencies to help meet critical milestones.…

Read More
Blog

3 Strategies to Successfully Engage Participants in Your Trial

Engaging participants and creating a positive experience throughout your clinical trial increases protocol compliance, participant…

Read More
Blog

Study Activation Survey Results: Budget Negotiation

Budget negotiations reveal hidden costs and extended timelines, underscoring the importance of efficient processes for…

Read More
Blog

Study Activation Survey Results: Medicare Coverage Analysis (MCA)

MCA timelines impact trial activation efficiency, with staffing shortages a key barrier. Many sites find…

Read More
Blog

Enhancing Diversity, Equity, and Inclusion in Cancer Research: Overcoming Challenges in Clinical Trials

  Diversity, equity, and inclusion (DEI) are critical pillars in the evolving landscape of cancer…

Read More
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

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