The system for ensuring that medical devices meet the necessary standards, specifications, quality, safety and performance requirements is complex. Understanding EU legislation, they key regulatory actors and the essential steps in the CE marking system is vital to bringing products to market.
Our training and education resources include videos, infographics, position papers, workshops and direct engagement with members and national industry associations.
Who is this course for?
Managers in healthcare institutions
For participants who are already familiar with medical technologies, the goal is to remove certain doubts, provide necessary information about medical technologies, show certain solutions from practice, from assessment practice, as well as enable a free exchange of experiences between participants and lecturers. Participation in this seminar is a form of professional training for personnel who use medical devices and medical technologies on a daily basis.
Our trainings are developed by subject matter experts to help organizations and individuals improve personal competence and skills - core enablers of sustainable business development and competitive advantage.
Innovations in medical technologies are one of the leading areas of economic growth in the world.
This course aims to provide knowledge of the concepts, data, and methodology required to manage medical devices and inventroy in healthcare institution and to ensure regulatory compliance to international and national requirements.
Training programme according to ECRI and Fluke Biomedical guidelines.