Carlos Pinto, Medical Device Executive, Med-Di-Dia
Carlos is a Regulatory Affairs and Quality Consultant at Irish MedTech Regulatory Consultancy Med-Di-Dia Ltd. He has 13 years of experience in a wide range of regulatory affairs related to microbiology, biotechnology and laboratory techniques.
Carlos is an alumnus of Newcastle University and Hull University in the United Kingdom. For the last 6 years, he has given proven regulatory solutions in the MedTech space and helped different medical devices to enter the market. With his extensive knowledge and experience, Carlos's expertise promises end-to-end regulatory and quality support for the MedTech community.
This session will walk you through the different types of Economic Operators as defined by the EU IVD and Medical Device Regulations highlighting how critical it is to understand these roles, and associated responsibilities, within the supply chain. These new regulations have increased the number of mandatory requirements which now need to be met. Carlos Pinto from Med-Di-Dia Ltd will cut through the maze of requirements, and regulatory jargon, to help attendees formulate strategies to implement controls within the supply chain.