In this special episode of the comedy podcast, host Subhi Sade welcomes Munir Al Azouzi, the founder of Easy Medical Device. Munir shares his expertise on the often confusing topic of the EU’s Medical Device Regulation (EUMDR), focusing on the distinctions between roles such as legal manufacturer, distributors, importers, authorized reps, and persons responsible for regulatory compliance. Munir explains the need for compliance checks, supply chain management, traceability documentation, and regulatory responsibilities in the context of the EUMDR. He also discusses his company's role as an authorized representative, importer, and consultant, and the various services they offer to help medical device manufacturers navigate regulatory complexities. 00:03 Introduction and Guest Introduction 01:47 Understanding the Economic Operator Model 07:56 Legal Manufacturer 09:41 The Role of the Authorized Representative and PRRC 23:39 Understanding the Role and Responsibility of Authorized Representatives 26:14 The Role of Importers and Distributors 27:38 The Importance of Traceability in the Supply Chain 38:14 Terminating a Mandate with a Manufacturer 40:55 Conclusion and Easy Medical Device Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies and particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people have a better understanding of the Medical Device Regulations all over the world. He now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through Videos, podcasts, online courses. Easymedicaldevice.com