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The tasks that the Medical Affairs department manages include identifying and assessing risks and medical risks as well as creating medical reports. The department also issues clinical evaluation reports and provides support in periodic safety update reports.
After they receive market approval, medical products are subject to intense monitoring: information about the safety and performance of devices is proactively collected, analyzed and processed. Adverse effects are reported to the regulatory authorities. When the need arises, the colleagues in Medical Affairs assist the corporate safety officer in consultations with the appropriate authorities and in processing safety data and corrective measures.
Degree in nutrition, biology, pharmacy or medicine.