Latest CRO Resources

Why do Recruitment Efforts Fail to Enroll Enough Participants?

Despite heavy spending on patient recruitment, meeting enrollment goals is a huge challenge in clinical research, affecting sponsors, CROs and sites.

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5 Steps to Follow When Shopping for a Validated EDC System

Shopping for a validated EDC system can seem like a daunting task. Learn five steps that make the process less confusing.

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Why It’s Time to Make the Switch from Paper to EDC

Still using paper to collect and store your clinical data? Modernize your data management and make the switch to electronic data capture.

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Tips for Writing Effective Edit Checks in eCRFs

Shannon Roznoski of Forte shares tips for writing effective edit checks in electronic case report forms (eCRFs).

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Developing Case Report Form Creation SOPs in Data Management

Tina Lambert shares the Data Management side of creating separate SOPs for CRF creation in EDC and non-EDC systems, and their supporting documents.

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Do SOPs for Data Collection Equal Compliance with 21 CFR Part 11?

Anders Lindquist clears up common confusion surrounding standard operating procedures and 21 CFR Part 11.

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8 Must-Have Competencies for the Clinical Research Professional

Many professions have well-researched, clearly defined competencies that are essential for everyone involved — clinical research is no exception.

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How to Find Studies in Today’s Competitive Market

Improve your business development strategy by considering these key factors when finding new studies for your site.

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Beginner’s Guide to Clinical Trial Performance Metrics

Basics to help you get started measuring and improving your clinical trial performance.

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Designing CRFs for the CDASH Demographics (DM) Domain

Shannon Roznoski of Forte explains how to design electronic case report forms (eCRFs) using the CDASH standard for the Demographics (DM) domain.

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