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