Medical Devices Training Courses

We offer training solutions in a variety of delivery formats to suit your individual requirements. You can learn online at your convenience, join your industry peers in face to face public courses, or schedule in-house training designed to meet the specific needs of your organisation.

Understand critical changes regarding the EU MDR and find out about implementation timescales with this eLearning course.

Be involved in your organisation’s transition from Medical Device Directive 93/42/EEC to the EU MDR.

Gain the knowledge and skills necessary to understand the requirements of this standard, and learn how to perform audits to maintain and improve your quality management system.

Understand the technical documentation requirements of MDR 2017/745 so you can get your files right the first time.

Gain a comprehensive introduction to the key elements of risk management for medical devices and a practical foundation in the relationship between risk management, regulatory requirements and your quality management system.

Gain the knowledge and interpretive skills necessary to understand and implement the requirements of the new MDR 2017/745 and Med Dev 2.7.1 Rev 4, Clinical Evaluation in relation to expectations for clinical evaluations. Understand the changing landscape of regulations related to risk management with the objective of increasing patient safety.

Understand the critical changes in relation to EU IVDR and find out about implementation timescales with this eLearning course.

Gain the knowledge and skills necessary to perform first, second (including supplier) and third party audits of ISO 13485:2016 quality management systems.

Through SGS Academy, we provide training solutions to help organisations improve personal competence and skills, enable sustainable business development and gain a competitive advantage. With expert trainers who are experienced practitioners in their field, our training moves beyond theory, providing valuable real-world insights.