Medical Devices Training Courses

Scientists looking at DNA sequence

Stay up to date with the latest standards and regulations for medical devices with training from the SGS Academy.

Whether you want to understand the new requirements for the Medical Devices Regulation (MDR); updates to the In Vitro Diagnostic Medical Devices Regulation (IVDR) or implement and manage an effective medical device quality management system (ISO 13485), the SGS Academy’s qualified experts will deliver training to guide you through the constantly evolving and complex medical devices landscape. SGS Academy training courses will help you to understand the new developments and show you how to mitigate the challenges you will face, helping you to remain competitive in the market.

Learn more about our courses. Contact an SGS Academy specialist.

Our 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.

Introduction to the New MDR – Online

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

MDR – Implementing the Changes

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

ISO 13485:2016 Internal Auditor

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.

Construction of a Technical File in Line with MDR

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

ISO 14971 and 31000 – Adopting a Product and Process Risk-Based Approach

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.

Medical Devices Clinical Evaluation Implementation

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.

Introduction to the New IVDR – Online

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

ISO 13485:2016 Medical Devices Auditor/Lead Auditor Training Course

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

Why SGS?

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.

Training experts

Our expert trainers are experienced practitioners in their fields.

Global network

Benefit from consistent training throughout your organisation – anywhere in the world.

Tailored solutions

We deliver customised training that meets your exact requirements.

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