Adam Kijowski

Adam Kijowski is a Clinical Compliance Manager at Geistlich Pharma AG, where he hosts clinical processes. He is responsible for compliance review, generation, and approval of a variety of technical documents for devices in different medical areas. Discussions on clinical strategies for regulatory submissions and problem-solving for MDR certifications are his main activities.

Additionally, Adam supported Clinical Evaluation conduct of more than 800 medical devices of a variety of classes, ranging from Class I Rule I to Class III implantable of animal origin (both under MDD and MDR). He is experienced in PMS and Risk management. Adam holds a PhD in Molecular Cell Biology.