Med-Di-Dia Limited

Med-Di-Dia, a regulatory affairs and quality compliance consultancy focusing on the Medical, Digital Health and Diagnostic sectors of the European Life Science Industry. With passion and drive, we have the flexibility to provide a cost-effective, bespoke solution that exactly fits the needs of you, the client. Time-critical services: - Person Responsible for Regulatory Compliance For micro and small companies, we will be your Person Responsible under the new EU Medical Device and In-Vitro Diagnostic Regulations. #PRRC - European Union Authorised Representative For non-EU and UK companies, we can be your Authorised Representative within Europe. #EUAR / #EAR - Legal Representative...

Regulatory affairs,quality compliance,medical devices,digital health,diagnostics,eu authorised representative,eu person responsible,eu legal representative,technical files,regulatory strategy,clinical investigations,clinical evaluations,design files,design control,software validation,risk management,iso 13485,quality management systems,corrective and preventive action (capa),product classification,quality management,person responsible for regulatory compliance,cyber security,internet of medical things,european union authorised representative ,iomt,internet of medical things,samd,artificial intelligence ,machine learning,and cyber security

Med-di-dia limited operates in the Medical equipment manufacturing industry.

Med-di-dia limited's revenue is 11m - 100m

Med-di-dia limited has 11 - 50 employees.