Francesco Ambrosio is a highly experienced consultant in the field of borderline medical devices, with a particular focus on devices based on herbal substances for wound management. He is skilled in CE marking and regulatory compliance with medical devices directive 93/42/EEC and MDR 745/2017, as well as in conducting audits and managing risk in compliance with ISO 14971. Ambrosio is also a lead auditor in ISO 9001 and ISO 13485.

Ambrosio has substantial educational background in the field of medical devices and healthcare, having studied medicinal plants and phytocellular products, technology assessment in healthcare, and chemical engineering. He has worked with various organizations in different roles including Senior Lecturer, Sales Director, Manager in Quality Assurance, R&D Engineer, and R&D Scientist.

He has a strong background in quality control and quality assurance, having worked as Quality Control Manager Assistant at SVAS Biosana S.p.A, and as a Quality Assurance consultant at TQM. He has also worked in the military for the Italian army as a Lieutenant.