Julian Thorns has over 20 years’ experience in the medical devices industry and has served for more than 15 years as a consultant at NSF PROSYSTEM GmbH.
In his current role as Principal Consultant, he is responsible for the operations of the business.
In addition to his qualification as lead auditor, Mr. Thorns 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.
Mr. Thorns 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. Strategic consulting and support for authority inspections (including the MDSAP) are his core competencies.
Mr. Thorns serves as a trainer at different organizations, such as TÜV SÜD and DIN (German Institute for Standardization), in a range of areas, including international regulatory affairs, risk management, technical documentation, the MDSAP and more.