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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 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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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

ryze training session

Our ryze training and CDISC support services - all you need to know

Clinical research

Achieving CDISC compliance in academia

Everything you need to know about CRFs

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?


Using CDISC to Optimize Clinical Study Set Up