Julian Thorns has over 20 years’ experience in the medical devices industry and been a consultant for more than 15 years. In his current role as Principal Consultant, he is responsible for the operations of the business.
In addition to his qualification as lead auditor, Julian advises many established companies in the medical industry and offers expert support for the implementation of current regulatory frameworks, such as the new EU-MDR and EU-IVDR.
Julian focuses on national and international registrations for medical devices and related technical documentation, human factors, risk management, post-market surveillance and vigilance as well as quality management and project management. His main competencies also include strategic consulting and assistance with authority inspections, including the MDSAP.
Julian is a trainer at different organizations in a range of areas, including international regulatory affairs, risk management, technical documentation, the MDSAP and more.
Areas of Expertise:
- Regulatory Affairs
- Technical Documentation
- EU Medical Device Regulation (MDR)
- Risk Management Systems
- Usability and Human Factors
- Quality Management Systems
- Audits and Inspections