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Features of Formedix Ryze Clinical Trials Software for Efficient Process Automation

 

Find it challenging to apply the clinical trial results or get stuck with a huge pile of the needed information? Indeed, dealing with clinical metadata, collecting, storing, analyzing, and managing can become a real challenge for an experienced data analyst and biostatistician. Thus, to solve such issues, medical researchers can use specific software that compiles, standardizes, and automates the clinical studies in one place. Applying the Formedix Ryze platform to design and build the needed data easily and faster.

 

Formedix Ryze clinical trials software will unify your clinical study outcomes after you publish them on the peer-reviewed sites and after they’re examined by the field experts. Be sure that this software will preserve data reliability and will fully meet the FDA requirements for clinical trial registration.

 

It’s a well-known fact that when conducting clinical research, it’s obligatory to publish and submit that scientific information to credible database sources. It’s a must to know what study design and data analysis to apply to resonate with the demands of the FDA.

 

Also, researchers must summarize the outcomes in a tabular format. If all these requirements are a hassle to you, never mind, you can get a unique opportunity to polish the clinical study layout and collect the outcomes with the help of the Ryze platform.

 

Ryze Overview: Its Peculiarities and Perks for Users

 

So, what is the Ryze clinical trial software? This is an advanced automated cloud CMDR (clinical metadata repository), which uses the specific tools to standardize clinical study and reuse the needed trial from diverse e-clinical systems without wasting time on manual management and arrangement.

 

Ryze will suit your objectives if you need to visualize CRFs, tailor EDC with the defined functionality, craft annotated CRFs, or approve your trial. How will the Ryze software promote your clinical study?

 

  • Sharing the outcomes within the team and cooperating with other medical researchers and data analysts.
  • Having data standardized so it’s possible to reuse already existing databases and annotations.
  • Saving time by exporting your trials into the EDC system.
  • Previewing CRF design before the final submission.
  • Data conversion to SDTM before conducting a study.

To guarantee smoothly visualized, annotated, and approved CRFs, and add scientific weight and data management capabilities, ryze software has fitting tools to vouch for the more precise and appropriate results:

 

  • Access to clinical MDR to reuse the data.
  • Annotated CRFs to reuse in your trials and save time.
  • Compliance with CDISC criteria, including FDA and NCI.
  • API integration with other programs to automate data processing.

 

What’s more, you don’t need to install Ryze because it’s cloud-based software that is on deck wherever you are. Thanks to onboard CDISC standard templates like SDTM, SEND, ADaM, NCI, etc., your research will be checked for compliance with the defined terminology and norms as well. With Ryze, you’ll be able to check and edit your trial in real-time, so you’ll see how the chosen CRF fits your EDC. Hence, it’s absolutely possible to design the structure and manage and control it in the Ryze platform.