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

Posts by: Gilbert Hunter

Gilbert Hunter
Gilbert joined Formedix nearly ten years ago as a technical writer. The system knowledge he gained from content development, together with his existing customer service skills, marked him out for transition to the Professional Services (PS) team. Gilbert has worked with the PS team for over four years, providing both CDISC-based training and software training, as well as support and consultancy services to Pharmaceutical, Biotechnology and Clinical Research Organizations. He helps organizations build studies faster and to a higher quality by making their clinical trial design and regulatory submissions far more efficient. Today, as Customer Success Manager, Gilbert’s focus is to ensure customers maximize the benefits they can achieve from ryze by overcoming their challenges and achieving their goals.
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What should a clinical MDR do?

How to Choose and Implement a Clinical Metadata Repository

Clinical trial technology

How clinical trial technology can streamline the research process


Streamline your clinical trials with automated metadata management

CDISC standards header image

A guide to CDISC standards used in the clinical research process

Clinical research

Achieving CDISC compliance in academia

What You Need to Know About CRFs in Clinical Trials

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


4 Reasons Why You Shouldn't Ignore CDISC Data Standards


What to consider when working with CRFs in clinical trials

Compliance, regulations, standards for Clinical Trials

Using SDTM, ADaM, and SEND for Regulatory Submissions


Using NCI controlled terminology for standardizing data


How CDISC standards fit into the drug development process


Introduction to CDISC Standards


Why switch to automated CRF annotations?