Risk Minimization Activities (RMA)

13 December 2018

Recent biological medicines often require closer follow-up of the patient.

Remedus guarantees the follow-up of the demanded vital or non-vital parameters at specific moments in time. The adjustable software platform Remecare allows us to follow all patients via a dashboard and monitor them. In case of abnormalities, we can take action. We perform different kinds of point-of-care tests (blood examination, urine analysis, spirometry…) and make relevant information accessible to health-care professionals in Remecare at all times. On the basis of the rules and algorithms which have been established, the platform will also notify the health-care team if an intervention is necessary. Solid medication security processes for the pharmaceutical industry are embedded in Remedus’s way of functioning.

Remedus is ISO 13485 certified (design and production of medical devices). Our product, Remedus Software Suite, is CE certified in accordance with the European directive concerning medical devices (93/42/EEG) and is used for the telemonitoring of patients’ vital and non-vital parameters at home.

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