Training courses, templates & coaching for professionals working within the medical device industry
Become more confident in medical device product development. Join thousands of medical device professionals that take our highly-rated public and customised blended (online + live virtual class), classroom and online courses. Topics include risk management, design control, project management, quality management, software development, usability engineering, safety for medical devices, clinical investigation and the Medical Device Regulation.
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Direct access to authors of the standards
Our courses are developed by members of the standardization committees, ensuring you receive up to the minute, first-hand information. Gain insights by learning from those who author the standards.
Training effectiveness and record-keeping
We measure our training’s effectiveness by assessing participants' knowledge throughout the course. We provide records, including course certificates to satisfy ISO 13485 requirements.
Emphasis on implementation of requirements
Our courses go beyond explaining requirements. We guide you to implement them effectively.
Understand and meet requirements with practical strategies.
- We have been a member of the CPD Standards Office since 2024, and our training courses are CPDSO-accredited. Upon completion of any of our courses, you will receive a certificate awarding you CPD points.
Blended courses (online + live virtual class)
Our state of the art blended courses combine online training with live virtual classroom sessions, led by an industry expert. This way, the theory is learnt first at your own pace, before being put into practice, using case studies and real-life scenarios, during the classroom session. The online training can be started immediately. We currently offer this type of course for Design Control for Medical Devices, Project Management for Product Development of Medical Devices, Risk Management for Medical Devices, Safety for Electrical Medical Devices, Medical Software Development, and Usability Engineering.
Learn how to develop new medical devices and maintain them in organisations where design control requirements apply.
The course covers both European and US requirements.
Learn about writing medical device user needs and design input requirements, gain insight in importance of documenting and managing requirements, user needs, and design inputs when creating medical devices.
Course length approx. 15-29 hours
Participant limit 8
Learn how to work with risk management according to the ISO 14971:2019 standard. It also includes an orientation on the ISO 14971 risk management’s relation to tools and techniques such as FMEA and P-FMEA.
Course length approx. 13-23 hours
Participant limit 8
Learn how to identify and manage product specific requirements and how this process is integrated with the design control and risk management processes. The course covers the IEC 60601 series of standards.
The course is focused on the process of developing software for medical devices. It covers the IEC 62304 standard itself and in relation to other standards such as ISO 14971, IEC 60601-1 and IEC 82304-1.
The course covers topics of general requirements of usability engineering, use specification, establishing user interface specification and evaluation plan, user interface design, and performing formative and summative evaluations.
Templates
Click on the button to view the full range of our expertly crafted professional templates which will help you create the required documentation to meet ISO 13485 or QSR requirements.Articles
Find fresh and useful information, tips and tricks regarding project management, product development and design control from professionals in the medical device industry.Online courses
Our high quality, self-managed, online learning courses can be completed in your own time. You have access for 6 months and can pause, resume and repeat as many times as you like! The course consists of pre-recorded lessons, quizzes and a final exam. Upon completion, you will receive a course certificate for your training records. Currently available are courses in Design Control, Usability Engineering, Safety for Electrical Medical Devices, Risk Management, Software for Medical Devices, SAMD, Medical Device Regulation, Quality Management, Requirements Engineering, Introduction to Working in the Medical Device Industry and Project Management.
Learn how to develop new medical devices and maintain them in organisations where design control requirements apply. The course covers both European and US requirements.
€ 399
Learn how to conduct internal and supply chain audits according to ISO 13485 and ISO 19011, and using remote auditing methods according to ISO TS 17012.
€ 499
Learn how to plan and document software development with the course covering IEC 62304 and IEC 82304-1 regulatory requirements, cybersecurity management, cloud and AI.
€ 499
This online course focuses on identifying and managing applicable safety releated requirements throughout the design control process.
Course length 9-25 hours
€ 449
Course focused on how to work with risk management according to the requirements of ISO 14971:2019 standard.
Course length 6-16 hours
€ 399
Learn how to be effective in medical device software development with IEC 62304 standard, and apply it to your projects.
Course length 9-25 hours
€ 449
How to Online courses
Our short courses focus on single topics and explain real-life scenarios and working with templates available on Medical Device HQ platform is a great way to introduce yourself to the flow and structure of our regular online courses. Currently available are the course on creating a Design and Development Plan, and course on creating a Risk Management Plan.
Course focused on how to create a design and development plan based on a Medical Device HQ template and address the requirements in 7.3.2 in ISO 13485 and 820.30 in QSR.
€ 49
Course focused on creating a medical device risk management plan that meets the requirements of ISO 14971:2019, MDR and QSR based on a free Medical Device HQ template.
€ 49