Cardioreport allows heart centres to easily fulfil its regulatory obligations, by providing registry reporting functionality. Users are intuitively guided through the requirements of the dataset by the software. Visually the software helps the users understand which information is required by the registry by highlighting the missing information. Each registry requirement is fulfilled by validation rules within the procedure reporting process, meaning that the report cannot be signed with missing data attributes. Cardioreport validation rules ensure that the data submitted to the registry is accurate.

Cardioreport collects the information in a structured manner ensuring no duplicate data is entered and sent. With the data being stored in the database it can be retrieved and viewed at any time required by the hospital management.

Registry data can be manually exported from the system for submission. In some cases the receiving systems will allow direct interfacing with CardioReport for seamless data submission.

Registries and Accreditation

(but not limited to)

  • ARS, SFC
  • AQUA
  • QERMID
  • CRAC
  • CCAD
  • NICOR
  • BCIS
  • CRM
  • EP
  • MINAP
  • HF
  • CONGENITAL
  • NCDR US dataset complient
  • Meetbaar
  • BQS
  • GISE
  • PCI French registry
  • PCI Swiss registry
  • PCI Austrian registry
  • TAVI French registry
  • CARDS

about

Us

Founded in 1995, MediReport Company is now a European market leader providing a complete Cardio Vascular Information System (CVIS) that comprehensively integrates invasive and non invasive cardiology, clinical procedure capture, hospital record and supplier inventory management. MediReport is focused on design and development of its advanced software solutions. The functionality, specifications and utility of the system is designed, directed and tested by a panel of physicians, while the software development is performed by a team of highly skilled in house software engineers.

 

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