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See how our new cloud-based platform can transform your clinical trials.

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Automation you’ll love. Standardization you’ll love...


See how CRFs look in Rave, InForm and leading EDCs – as you design in our clinical MDR.

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Easily comply with ever changing CDISC standards & NCI Controlled Terms.

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Join our webinar to hear about UCB’s metadata automation journey.

Thursday March 04 2021 | 12pm EST / 11am CST / 9am PST 60 min SEE AGENDA & REGISTER

Get clinical trials designed, built & submitted, faster with our clinical metadata repository & automation platform

Get the job done quicker with our clinical metadata repository (MDR) and clinical trial automation software. We’ve automated those time-consuming and expensive manual tasks. Everything from study set up to submission. So now you get clinical study build much faster than before. CDISC compliance is taken care of too – all in one place.

Formedix is available straight out-the-box. So whether you need a clinical metadata repository, or help with study automation, you’re ready to go RIGHT NOW.

Increase margin – improve profits

You get clinical trials started, built and submitted much faster with Formedix. This makes it possible to launch products much sooner, and also run more trials. That’s a real opportunity to increase revenues and profits.

Cut the cost of running trials

Formedix automatically does the time consuming manual stuff for you – often at a click of a button. From Building your EDC, to creating a define.xml file… we make it happen. Fast. As a result, you save loads of time & resource, so it costs you less to get the job done.

Be way more efficient

No matter where you are, you and your teams can easily find content in 1 central metadata repository. You won’t lose time searching for what you need. Go to 1 place to instantly find, use and share content.

Improve compliance & data quality

We help you fully comply with the latest FDA and NCI standards. This includes upgrading our platform with new versions of CDISC, so that you’re always compliant. Formedix makes it easy to use standards consistently, and validate that your content is correct too.

Clinical metadata repository

Trial building and managing clinical studies is tricky. And very time consuming. We help by speeding up the end-to-end clinical metadata process, and making it much easier. With our clinical metadata repository, all your content is in one place. And it’s all fully connected, from forms through to submission content. You can easily find, review,  manage, reuse, and share content – even across different EDC and e-clinical systems. Plus, it’s off-the-shelf, so you can get started, fast!


Clinical trial automation software

Don’t need a clinical metadata repository? Our study automation platform gets things done quicker and easier. Whether you want to build EDCs, create define files, annotate CRFs, convert datasets, or validate your study… our clinical trial automation software and metadata repository tools makes it quick and painless.

What can I do with Formedix?

How can our platform help you?

Build studies faster - import/export from EDCS

Export your study into your EDC system, straight from Formedix. And if you’re using Rave or InForm, you can import studies right back into Formedix to make any changes. Even do complex edit checks and visit structures. 

Preview CRF Designs

See what forms will look like in your EDC system at the push of a button. Not happy? Go back, make changes, then preview again until you’re done.

Save time by reusing clinical metadata

Reuse content from one study to another study – even across multiple EDCs. Reuse forms, edit checks, datasets, standards, mappings, annotations… No need to re-type stuff, so you save loads of time.  

Get SDTM datasets before trials start

Formedix shows you what your source dataset column headings will be – even before you’ve collected any patient data. So you can do your mappings early on too. By the time you get trial data back, your datasets are all mapped, and it’s just 1 click in Formedix to convert to SDTM.

Cherry pick your EDC - don't be tied in

Choose your preferred EDC for your clinical trial building. Even use a different one for each study phase. We integrate with 7 systems, including Rave, InForm and TrialMaster. This gives you huge flexibility – you’re not committed to using a specific EDC system. Mix it up, however you want.

Build your EDC study in 1 click

Happy with your forms? Now it’s 1 click to build you EDC. Formedix automates the build process, saving tons of time, so you can start your trials much sooner. 

Effortlessly comply with standards

No worries about meeting regulatory standards. Formedix is built on the latest CDISC compliant templates. That means you automatically comply with FDA and NCI standards. 

Easily share content & collaborate

Share content and work together from anywhere.  The Formedix repository keeps everything in 1 place, allowing teams to work more effectively and efficiently.  


instead of 1,484 EDC labor hours


instead of 486 SDTM labor hours


weeks instead of 20 for EDC go-live


weeks instead of 8 to see SDTM data

What can Formedix do for me?

We help pharmaceutical and life sciences teams manage clinical metadata more easily – and get more done! By getting rid of long manual processes, and building in compliance throughout, we make life just that bit easier!

What is a clinical metadata repository?

Our clinical trial automation software incorporates a clinical metadata repository. Its core features help speed up the clinical trial process, and bring life-saving products to market, faster.

Your whole team can access all your standards and studies in one place, on the web. For example, you can control access, assign work to individuals, allow parallel review, perform impact analysis, and version all of your content.

Global search functionality makes it quick and easy to find studies, standards, and assets in your metadata repository. This gives greater transparency, control and better communication amongst your team. In doing so you produce higher quality study designs, which gives you more consistent data for your submissions.


Build CRF designs faster, in many different EDC systems

Why we're different

It takes a fraction of the time to set up your study in Formedix compared with other systems. If it normally takes 20 weeks to have your EDC study ready, it can be as little as 4 with Formedix. And the sooner you start trials, the sooner you submit your study.  

We’re the only commercially available off-the-shelf clinical metadata repository. Straight out the box and off you go – we don’t have to custom build it for you from scratch.

Only we integrate 100% with Rave and InForm. So as well as seeing what eCRFs will look like before you build your EDC, you can do complex edit checks and visit structures too. Want to re-import data back into Formedix? No problem, you can do that too!

Some companies don’t improve or expand their platform. We do, constantly. We’re always working on new automation stuff, and it’s based on your feedback.

No other platform automatically builds your study in just about any EDC system – 7 to date – saving loads of time. Use your favourite, or even different EDCs for different studies.

Ours is the only fully integrated clinical metadata repository. There’s other clinical metadata repository’s, but they don’t connect with other EDCs or e-clinical systems. We’ve put everything in 1 place, where your content is truly interconnected.

Nobody supports full end-to-end metadata like we do. We cover it all – forms, edit checks, proprietary datasets, mappings and analysis results metadata. And we support every version of CDISC & NCI standards.

Unlike others, you can truly reuse content across multiple EDC systems. Simply drag and drop content from 1 study to another, or one standard to a study – regardless of system. 

Some of the organizations using Formedix



Effortless CDISC compliance

We manage your CDISC compliance. So you don’t have to.


Don’t worry about meeting the latest FDA data standards. Formedix supports all versions of CDISC standards. And we keep our platform updated in line with CDISC and NCI standards. That way your study designs and datasets are always regulatory compliant.

As one of the first CDISC members back in 2001, you can rely on our deep rooted knowledge of all things CDISC. We’re members of the CDISC XML technical team. As such we’ve been involved in developing many key features in CDISC ODM and Define models. This makes us well placed to give real-world, practical CDISC training. See our CDISC membership certificate for the year 2020-2021. Click below to find out more.  

Got a project in mind?

Tell us what you’re trying to do, and we’ll show you how we can help.