Jeeva is currently pursuing a Master’s degree in Medical Systems Engineering at Otto von Guericke University Magdeburg. At IKIM, he supports the Regulatory Affairs and Quality Management team as a Student Assistant, with a focus on Software as a Medical Device (SaMD).
In this role, Jeeva contributes to the implementation of regulatory strategies and compliance processes. He supports the maintenance of the Quality Management System in accordance with ISO 13485, risk management activities according to ISO 14971, and software lifecycle activities in accordance with IEC 62304.
In addition, he contributes to the preparation and maintenance of regulatory and technical documentation, thereby supporting the regulatory compliant transfer of medical software from research into clinical application.
