Medical Devices Training Courses from SGS

Cardio Monitoring System

Gain the skills and knowledge to maintain compliance with latest medical devices training courses.

The medical devices industry is one of the most heavily regulated. Training your staff is key to ensuring compliance, being aware of risks and aligning your activities with international regulatory requirements. Whatever your role, you need to make sure you get it right.

Expert trainers

Designed and delivered by subject matter experts, our training courses are interactive and every session draws extensively on the trainers' experience, including practical examples. 

From face-to-face, Virtual Instructor Led Training (VILT) or eLearning you can access a wide range of courses delivered in many languages.

Certification 

With SGS course completion certificates you can expect the highest levels of recognition within the industry, supporting career progression.

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Medical Device Training Courses

Medical Device Regulation Internal Auditor Training

Understand Medical Devices Regulation (EU) 2017-745 and how to conduct an internal audit against its requirements.

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ISO 13485:2016 Medical Devices QMS Lead Auditor Training

Acquire knowledge and skills to perform audits of a MD QMS against ISO 13485:2016, in accordance with ISO 19011 and ISO 17021, as applicable.

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Medical Device Regulation Implementation Training (EU) 2017/745

Understand the additional requirements within the Medical Device Regulation as well as those of the current directives and ISO 13485, including the terminology used and certification requirements.

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Medical Device Regulation Technical Documentation Transition Training

Learn about the technical documentation requirements of the Medical Device Regulation and understand what notified bodies are looking for.

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Medical Device Regulation (EU) 2017/745 Clinical Evaluation Implementation Training

Understand and implement the requirements of the Medical Device Regulation and clinical evaluation in relation to expectations for clinical evaluations.

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Medical Device QMS Software Validation Training

Acquire the knowledge and skills required to determine appropriate activities for the validation of process software used in medical devices.

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In Vitro Diagnostic Medical Device Regulation (IVDR) Technical Documentation Training

Learn about the technical documentation requirements of the In Vitro Diagnostic Medical Device Regulation and understand what notified bodies are looking for.

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ISO 14971:2019 Risk Management for Medical Device Introduction Training

Get an overview of ISO 14971:2019 Medical Devices risk management and how to apply it within your organization. Develop a broader understanding of the changing landscape of regulations related to risk management, with the objective of increasing patient safety.

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In Vitro Diagnostic Regulation (IVDR) Introduction eLearning

Gain an overview of the IVDR and understand the implementation timescales.

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Medical Device Regulation (MDR) Introduction eLearning

Gain an overview of the MDR and understand the implementation timescales.

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Why SGS Academy?

As a leader in professional training, we draw on years of worldwide experience to provide effective learning and development opportunities, nurture talent and enable continuous organizational progression.

SGS is a Global Training Organization with extensive testing capabilities across all Medical Device categories. We are a designated UKCA Approved Body, a CE Notified Body and a recognized MDSAP Auditing Organization.

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