We help the development and sales personnel to understand the end users and the operating environment of the devices. We familiarize the personnel with the different areas of healthcare and deepen peronnel's understanding of healthcare practises. Mainly this training take place in real healthcare environments by healthcare professionals.
We also offer accredited training focused on medical device requirements with our partner, Comply Guru. Our training covers the key legislation and requirements of the industry, including ISO 13485 and ISO 14971 standards as well as MDR, IVDR, FDA QSR and MDSAP legislation. Education levels range from foundation to lead auditor. Comply Guru holds the accreditations with CQI & IRCA (ATP No. 6081148) and Exemplar Global. eLearning (24/7) or blended learning formats are offered in the English language. See examples below and more details on our partner's website here or contact us.
For anyone looking to gain a comprehensive understanding of the core requirements of ISO 13485
8 hours Online, 595 € + VAT, Customer rating 4,5 *
For anyone that wants to be part of the team that performs internal audits of part of their Quality Management System (QMS) based on ISO 13485
16 hours Blended, 795 € + VAT, Customer rating 4,6 *
Comprehensive Practitioner Training that takes you through the new EU MDR 2017/745, not just from an industry perspective, but also from a Notified Body perspective
20 hours Online, 1.195 € + VAT, Customer rating 4,6 *
For anyone that wants to lead a full system audit of a Quality Management System (QMS) based on ISO 13485, auditing against ISO 19011, and/or ISO/IEC 17021 as appropriate
40 hours Blended, 1.595 € + VAT, Customer rating 4,7 *
*) Check the current price and other detailed training information on the website of our partner Comply Guru.