DLSIX CONSULTING advises and supports companies in the CE conformity of their products, compliance with regulatory requirements, project management, innovation and staff training.
DLSIX CONSULTING’s activities also include:
informing companies of the standards and regulatory requirements applicable to their products or services, and advising them on the choices and strategies to adopt in the face of these constraints
Advising companies on the standards and regulations applicable to their products (Medical Devices and Personal Protective Equipment) or services, and ensuring their compliance.
Authorized Representative (AR) services for medical devices manufacturers located outside Europe, in accordance with MDR (EU) 2017/745
Person Responsible for Regulatory Compliance (PRRC) services for economic actors (Manufacturers, Importers and Authorized Representatives), in accordance with MDR (EU) 2017/745
Support for project management, product or process development, partnership building (particularly through networking) and financial engineering of projects
Support in conducting scientific and technical studies and literature searches.