MED-RAS GmbH was founded in 2002, with the target to support businesses in the health sector in their compliance with legal requirements.
Key aspects of our work are
- Analysis, establishment and the further development of management systems
- Product risk analysis and risk management procedures
- Assistance with the product certification and performance of validations
- Advice and assistance with German, European and international licensing and/or registration of medical devices and especially with the application for their notification in the register for medical technical aids reimbursement list („Hilfsmittelverzeichnis der Krankenkassen“ -HMV) of the German health insurance funds.
Since the foundation of our company we have been able to deepen and expand our knowledge and experience in this diverse field. This enables us to call upon a team of experienced and competent staff and associates when processing assignments.
We open opportunities
To help open up new opportunities for your strategic business direction, we work with you to develop unconventional solutions to problems. We are able to integrate formal requirements of standards and directives into suitable and pragmatic work processes rather than inefficient model solutions, to enable you to gain the maximum benefit.