Claudia Mastrobuoni has over 5 years of Medical Device industry experience in both regulatory affairs and quality assurance. Claudia’s background includes experience in EU/UK market entry, UK Responsible Person and ISO 13485:2016 implementation. Claudia is responsible for supporting client projects including Clinical Evaluation Reports and Technical File builds. She is also responsible for managing Apotech’s UKRP, EU Authorized Representative and PRRC services, whilst also maintaining our internal ISO 9001 Quality Management System.
