Adrianna Pyrzanowska

Adrianna serves as a Regulatory Affairs Associate at Pure Clinical. She specialises in advising on the regulatory compliance of medical devices across various classes, including aesthetic and non-medical products covered by Annex XVI of the MDR, preparing technical documentation, managing device registration processes, and implementing quality management systems in accordance with ISO 13485. She gained professional experience at, among others, the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in Poland, as well as at consulting firms serving the medtech sector. At Pure Clinical, she supports manufacturers in successfully bringing their devices to the European market, ensuring compliance with MDR requirements and maintaining high quality standards.