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.
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.
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.
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.
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.
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!
Our clinical trial automation software incorporates a clinical metadata repository (MDR). 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.