Training Courses and Patches
A challenging and complex market as the medical one, with a continuous need of meeting necessary standard, regulatory requirements and maintaining high the quality, safety and performance of management systems, requires dedicated and focused training solutions. Understanding international standards, EU regulations and directives, and the essential steps in the CE marking system is vital to bringing products to market.
That is why Kiwa, through its training companies offer a comprehensive range of medical device training courses carried out in line with the company strategies and the social transformations of the health sector and of the production and marketing of medical devices.
For these sectors, training is structured in a timely and effective manner thanks to Kiwa's expertise acquired over the years in system and product certification, innovation and support for professional and institutional accreditation.
Our services in the field of training courses for medical devices
The aim of the training is to inform the participants about EN ISO 13485: 2016 Medical Devices Quality Management Systems and to train competent auditors who can take an active role in the audit cycle which is required by the standard. The partici...Show