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Blog

Key Efficiencies Driven by a Clinical Trial Management System

Find out how sites can get the most value from their clinical trial management system (CTMS) to streamline operations.

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4 min. read
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Webinar

FDA/OHRP Harmonization and Your HRPP Operations

This webinar will discuss the human research protection program (HRPP) opportunities and challenges through FDA and OHRP harmonization.

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Podcast

Decentralized Clinical Trials and Regulatory Changes

We discuss the evolution of decentralized trial modalities and possible solutions to regulatory challenges.

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Blog

Improving Diversity in Clinical Trials: Strategies for Inclusive and Ethical Research

Learn practical strategies on how to improve diversity in clinical trials for historically under-represented groups.

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5 min. read
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Podcast

My Favorite Case Study: COVID-19 Applications for Monkeypox

How the COVID-19 pandemic has shaped vaccine development, promoting accelerated research for conditions like monkeypox.

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Blog

Patient Recruitment from a Site Perspective: Technology Meeting Today’s Challenges

Discover how CTMS streamlines patient recruitment & management for successful clinical trials.

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3 min. read
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Case Study

University of Nebraska Medical Center Streamlines Regulatory Management and Accelerates Study Startup with Advarra eReg

Learn how Advarra eReg helps UNMC support remote monitoring and how eReg helped address prevalent challenges in clinical research.

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Webinar

Privacy and Confidentiality in the Age of Mobile Apps and Connected Devices

Discover how to protect participant privacy in mobile-app-based clinical research. Learn about risks and what IRBs need to consider in protocol review.

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Blog

Risk Assessment for use of Engineered Genetic Materials in Clinical Research

Learn why an institutional biosafety committee needs to complete a risk assessment for engineered genetic material in clinical research.

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4 min. read
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Webinar

Full Board vs Expedited vs Exempt: Why IRBs do That

A discussion on what IRBs must consider, what might tip the scales for a study that could go either way, and what “expedited review” means.

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Blog

eReg Benefits for Clinical Research: Use Cases for all Types of Sites

Using an eRegulatory system can benefit any site, helping to increase productivity, improve compliance, and save money.

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4 min. read
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Podcast

Diving into Single IRB Implementation

In this episode, we get an inside look at how institutions implement sIRB requirements and how to overcome potential challenges.

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