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

Philadelphia

CERTAINTY by Certara: May 2024 customer user group

What should a clinical MDR do?

How to Choose and Implement a Clinical Metadata Repository

Kevin Burges Volunteer Spotlight

Head of Product Management Kevin Burges - CDISC Volunteer Spotlight

Formedix ryze cloud based clinical metadata repository and SDTM automation suite and Certara Pinnacle 21 data validation platform combine to power faster clinical trials.

Certara acquires Formedix LLC to increase data standardization across clinical trials for faster study setup, time to analysis and submissions

Clinical trials day blog

Clinical Trials Day 2023: 276 years on from the first clinical trial

Formedix CORE desktop application

Easily validate clinical study data with Formedix CORE

Clinical data standards vs legacy data

Clinical data standards vs legacy data

Clinical research

Achieving CDISC compliance in academia

Free webinar: accelerate and improve CDISC SDTM deliverables

Webinar: Accelerate and improve the quality of CDISC SDTM deliverables

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Webinar: The Need for Standardization and CDISC

CDISC standards on laptop

Podcast: How CDISC compliant data accelerates drug discovery

A laboratory assistant in a laboratory with test tubes.

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

Accelerate-study-build-with-clinical-trial-automation-software

Accelerate study build with clinical trial automation software

ryze community event hosted by Formedix

Formedix to host ryze Community Event in Copenhagen in May 2022

CDISC-data-standards-formedix-blog

4 Reasons Why You Shouldn't Ignore CDISC Data Standards

Clinical MDR

CMDRs expedite drug development. So what’s holding the industry back?

clinical-software

Could Standardised Metadata be the Key to Optimising Clinical Trials?

ryze-software-for-clinical-study-build

What the Best Clinical Study Build Pros Do (and You Should Too)