Resources

EDC

Choosing an EDC: 9 Questions to Ask When Evaluating Vendors

With so many electronic data capture systems available, how do you know which EDC is the best fit for your organization? Consider these questions.

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[Q&A] Understanding, Achieving and Maintaining 21 CFR Part 11 Compliance

Expert webinar presenters answer attendee questions about 21 CFR Part 11 compliance and the validation process for electronic systems.

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Understanding, Achieving and Maintaining 21 CFR Part 11 Compliance

Watch this webinar to hear our expert presenters provide an overview of 21 CFR Part 11 and discuss the roles both organizations and vendors play during the validation process.

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Improve Data Quality with 5 Fundamentals of Clinical Data Management

Use these five fundamental elements of clinical data management to implement quality data practices across your research organization.

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Data Collection in Clinical Trials: 4 Steps for Creating an SOP

Learn the necessary steps to create an effective SOP for data collection in clinical trials.

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Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials

Medical coding dictionaries standardizes data interpretation, which increases data quality and minimizes risk.

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Report Card: Methods for Managing Lab Norms within your EDC System

How varying protocols and operations should change your organization’s approach to handling external data in your EDC system.

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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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5 Ways to Sell EDC to a Skeptic

Ready for an EDC system? Use these five points to generate buy-in from your leadership team.

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Introducing the Forte Research Ecosystem

Forte prioritizes customer community to develop collaborative solutions and meet the changing needs of the research industry.

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