With our global healthcare and medical expertise, we are able to offer specialised training courses for those working in the medical device sector. Our medical device training courses are focused on system legislation for manufacturers and distributors, in-depth studies on risk management, courses on product usability, CE markings, how to prepare to access non-European markets with your medical devices.
We also provide insights on regulatory requirements with a particular focus on new European Regulations 745/2017 (MDR) and 746/2017 (IVDR) which require companies that manufacture or distribute medical devices to effectively and promptly manage change.
Our courses are aimed at a range of roles including quality management managers in companies in the medical sector, healthcare professionals involved in the purchase or management of medical devices and operators intended for the regulatory / quality sector in medical companies. Consultants, evaluators and managers of the various business functions within the medical and healthcare sectors may also find our training courses useful.
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