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

Medical Devices: “Significant Risk” Versus “Nonsignificant Risk” Determinations

In medical device research, the determination of “significant risk” or “nonsignificant risk” is sometimes confusing,…

Read More
Blog

Diversity in Cancer Research: Getting Started

The most recent Cancer Center Support Grant (CCSG) guidelines released by the National Cancer Institute…

Read More
Blog

2022 Trends in Clinical Trials: Innovations, Participant-centricity, and Decentralization

In 2022, clinical research evolves with lessons from COVID-19, leading to new study designs, participant…

Read More
Blog

Research Involving Cosmetics: What you Need to Know

The Food and Drug Administration (FDA) is a U.S. public health authority within the Department…

Read More
Blog

Beginner’s Guide to Community-Based Participatory Research

With diversity, equity, and inclusion efforts currently at the forefront of the research community’s collective…

Read More
Site-Sponsor Consortium - an Advarra initiative
Blog

It’s Time for Sites to “Bring Your Own Technology” (BYOT)

Sites gain control with Advarra’s BYOT approach, eliminating redundant tasks and fostering efficient collaboration between…

Read More
Blog

The Clinical Research Training Program Checklist: What to Look For

Selecting a clinical research training program is crucial for ensuring compliance and success. Look for…

Read More
Blog

Critical Steps for Writing an Impactful Clinical Audit Report

The amount of detail required in an audit may vary – ranging from an executive,…

Read More
Blog

The Advantages of Outsourcing IRB and IBC Reviews to One Partner

Gene therapy studies are a relatively recent addition to the world of clinical research. As…

Read More
Blog

Understanding Various Decentralized Terms in Research

As many research organizations are becoming more patient-centric and adapting to technological advancements and remote…

Read More
Blog

Budgeting and Billing Compliance in Study Activation

Effective billing compliance starts with understanding routine costs, extended coverage, and administrative fees to avoid…

Read More
Blog

Navigating the FDA Emergency Use Filing Process

In an effort to create safe, effective, and affordable ventilators to help combat the foreseeable…

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