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Formedix

Formedix

Want to get your clinical trials designed, built & submitted faster? 

Formedix Platform

Now you can, with our off-the-shelf clinical metadata repository (MDR) and clinical trial automation platform. We've taken away those time-consuming and expensive manual tasks - from study set up to submission.

Clinical Metadata Repository

Our clinical MDR provides a central home for your organizational standards. Here you can manage, update, approve and reuse organizational standards. Whilst also keeping up with CDISC versions, and complying with regulatory requirements. You can even share and reuse content across different EDC and e-clinical systems.

We can help with automating study design and build. Our clinical trial automation tools use the content in your MDR to build your studies much faster. Whether you want to design eCRFs, build EDCs, design or convert datasets, or make define files… Formedix helps you do it in a fraction of the time.

Professional Services

You'll get a dedicated account manager who'll help you achieve your objectives, and make sure that everything runs perfectly with Formedix. This includes day-to-day support. If you want training or professional services, your account manager can provide this too.

Training

Become an expert in industry standards. Or learn the Formedix platform inside out. We can do on-site classroom training. Or, we can train you remotely through webinars. It's down to you and what's best for your needs.

Related resources

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How clinical trial software can optimize trials

How clinical trial software can optimize trials

Formedix | 09-Jun-2021 | Technical / White Paper

This article explains the different types of clinical trial software available, and how it can be used to optimize the end to end clinical trials design...

How a clinical metadata repository helps with data

How a clinical metadata repository helps with data

Formedix | 22-Mar-2021 | Technical / White Paper

This article covers the various ways a clinical metadata repository helps with data quality, and in turn, with data quality in the clinical trials process....