<img height="1" width="1" style="display:none" src="https://www.facebook.com/tr?id=905310923417895&amp;ev=PageView&amp;noscript=1">

Hi we're Formedix!
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.
Find me on:
    Clinical trial technology

    How clinical trial technology can streamline the research process

    Automated-Metadata-Management

    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

    CDISC-data-standards-formedix-blog

    4 Reasons Why You Shouldn't Ignore CDISC Data Standards

    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


    New Video-01

    Hear about argenx’s guide to clinical metadata repository vendor selection and go-live in our free webinar.

    Watch the webinar