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CDISC

Live demos of ryze Clinical MDR at CDISC US Interchange 2022

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Here you'll find guidance & insights on all those clinical metadata woes! Keep scrolling for more...

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Posts by: Gilbert Hunter

Gilbert Hunter
Gilbert joined Formedix over seven years ago as a Technical Writer. Four years ago, the knowledge gained from content development together with his customer service skills marked him out for transition to the Professional Services Team. In his current role, Gilbert provides CDISC and software training, support and consultancy services to Pharmaceutical, Biotechnology and CRO organisations. He helps them save time and money by making their clinical trial design and regulatory submissions more efficient.
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Annotated CRFs made easy

Regulatory requirements for annotated CRFs made easy

A laboratory assistant in a laboratory with test tubes.

Software for clinical trials: Why it’s important for drug discovery

CDISC-data-standards-formedix-blog

4 Reasons Why You Shouldn't Ignore CDISC Data Standards

crf-design-clinical trial

Everything you need to know about CRFs

cdisc-standards

A Guide to CDISC Standards Used in the Clinical Research Process

What-to-consider-when-working-with-CRFs

What to consider when working with CRFs in clinical trials

Compliance, regulations, standards for Clinical Trials

Using SDTM, ADaM, and SEND for Regulatory Submissions

nci-controlled-terminology

Using NCI controlled terminology for standardizing data

cdisc-standards

How CDISC standards fit into the drug development process

cdisc-standards-overview

Introduction to CDISC Standards

automated-crf-annotations

Why switch to automated CRF annotations?

clinical-data-management-annual-conference

Using CDISC to Optimize Clinical Study Set Up