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House of MDR helps maintain compliance after your medical device goes to market. We have top expertise and can provide through our cooperation network wide range of PMS services.
An important aspect of the MDR is to guarantee the safety of medical devices. Post-market surveillance is a continuous process of monitoring and collecting data on the safety and performance of medical devices after they’ve been released to the market.
Our experts have over 20 years of experience of pharmacovigilance and MD vigilance. Our services are
The medical device vigilance system mandatory in EU has to set up by manufacturer of medical device to protect public health and the health and safety of patients of medical devices through the introduction of field safety corrective actions and the reduction of the possibility of recurrence of a medical device-related incident.
