PATS, or to give it its full title of Patient Analysis and Tracker System, is a software system for clinical outcomes and data management that is designed to help clinical facilities track and analyze outcomes for a wide variety of procedures and treatments. Whether you’re talking cardiac surgery, cardiology and vascular medicine, or oncology, orthopedics and transplant, PATS is a highly effective tracking solution. Track long-term outcomes with PATS follow-up, and perform longitudinal analysis that will enable you to better harness medical data for the following:
Data ownership
Guaranteeing you total access to your locally stored data at all times, PATS sets about harvesting, auditing and packaging data for registry submission, and can help you achieve all of your clinical initiatives with its unparalleled data mining capabilities and graphical output analytics.
Fully customizable
The amazing thing about PATS is that it’s 100% customizable, and gives you the ability to add any number of modifications, at no extra cost. Able to accommodate existing and pre-defined databases, along with user-defined data sets or registries, PATS enables you to custom-build registries, each of which has unlimited data elements. Making it simple to add, delete and edit data elements, whenever you need to, PATS gives fantastic flexibility that means you can integrate your own questions and customize data sets. PATS can also be expanded to efficiently and effectively track and analyze outcomes for unlimited medical procedures or treatments.
Reporting
Here to help your company prepare regulatory-ready serious and non-serious safety reports for both clinical and marketed products, we promise to remain fully compliant with all company-approved operating procedures, at all times; right from the initial event capture, through to submission-ready regulatory forms.
Analytics
Different to single-case reporting, which involves only individual AE reports, aggregate reporting involves the compilation of safety information for a drug over a period of months or years. An important element of any pharmaceutical business, we’ll ensure that all clinical and marketed periodic reports for planned regulatory response, are developed accurately and efficiently, and include country-specific reports where appropriate.
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