AUTHOR

Quality and Regulatory Affairs Manager at Star

Lukasz is a seasoned professional with over 20 years of experience in the medical devices industry. Specializing in business and product development, device validation, regulatory affairs, and quality assurance, Lukasz is a certified lead auditor in ISO 13485 and a member of TEAM-PRRC. With his wealth of experience and expertise, Lukasz Kilianek continues to make significant contributions to the medical devices industry, ensuring the delivery of safe and effective products that improve patient outcomes worldwide.