Suggested region and language based on your location
Your current region and language
Showing 1-10 of 1085 results
This course will introduce learners to the fundamentals of practical auditing using the ISO 19011:2018 standard. An ineffective audit can mean...
Training & Qualifications
Our one-day foundation training course to the General Data Protection Regulation (GDPR) will help you understand how it could apply...
Training & Qualifications
Our Introduction to ISO 31000 training course will teach you how to manage organizational risk and help make excellence a...
Training & Qualifications
This course is designed to help professionals understand the critical updates and changes to ISO/IEC 27701, equipping them with the...
Training & Qualifications
This course is designed to provide you with knowledge of how the Medical Device Regulation (MDR (EU 2017/745)), standards and...
Training & Qualifications
This training course explores the requirements of the ISO 13485:2016 Quality Management System standard, discussing key principles and how the...
Training & Qualifications
Learn about the key requirements, concepts, and the overall process for CE marking under the Medical Devices Regulation (MDR). The...
Training & Qualifications
Gain the required skills to conduct a base-line review of your organization’s current position and implement the key principles of...
Training & Qualifications
Find out best practice for assembling Technical Documentation and QMS when placing Medical Devices (MD) on the European Union market...
Training & Qualifications
The Regulation contains detailed requirements that need to be implemented, and will affect all IVD manufacturers, importers, distributors and EU...
Training & Qualifications