Adrianna Pyrzanowska

Adrianna serves as a Regulatory Affairs Associate at Pure Clinical. She specializes in regulatory compliance for non-active Class I medical devices, preparation of technical documentation, product registration, and implementation of quality management systems in accordance with ISO 13485. Her professional background includes experience at the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, as well as consulting firms serving the MedTech sector. At Pure Clinical, she supports manufacturers in successfully bringing their products to the European market, ensuring MDR compliance and maintaining high quality standards.