Call us on: +44 203 7456 463

Medical Device HQ AB

CPD Standards Office Provider Number: 50513

Medical Device HQ AB is a CPD-accredited training provider, accredited by The CPD Standards Office, an independent CPD accreditation body. Learn what CPD accreditation means and how to get your course CPD accredited.

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Accredited Activities

<ul>
 	<li style="font-weight: 400">Advanced Risk Management for Medical Devices and ISO 14971:2019</li>
 	<li style="font-weight: 400">Agile Medical Device Software Development</li>
 	<li style="font-weight: 400">Clinical Investigation for Medical Devices and ISO 14155</li>
 	<li style="font-weight: 400">Design Control for Medical Devices</li>
 	<li style="font-weight: 400">Design Control for Medical Devices - Practitioner Training</li>
 	<li style="font-weight: 400">How to Create a Medical Device Design and Development Plan</li>
 	<li style="font-weight: 400">How to Create a Medical Device Risk Management Plan</li>
 	<li style="font-weight: 400">ISO 13485 Internal Auditor Training</li>
 	<li style="font-weight: 400">ISO 13485 Internal Auditor – Practitioner Training</li>
 	<li style="font-weight: 400">Medical Device Requirements Engineering</li>
 	<li style="font-weight: 400">Medical Device Requirements Engineering- Practitioner Training</li>
 	<li style="font-weight: 400">PRRC - Person Responsible for Regulatory Compliance</li>
 	<li style="font-weight: 400">Process Validation for Medical Devices</li>
 	<li style="font-weight: 400">Process Validation for Medical Devices – Practitioner Training</li>
 	<li style="font-weight: 400">Project Management for Product Development of Medical Devices</li>
 	<li style="font-weight: 400">Project Management for Product Development of Medical Devices- Practitioner Training</li>
 	<li style="font-weight: 400">Quality Management for Medical Devices and ISO 13485</li>
 	<li style="font-weight: 400">Quality Management for Medical Devices and ISO 13485- Practitioner Training</li>
 	<li style="font-weight: 400">Risk Management for Medical Devices and ISO 14971:2019</li>
 	<li style="font-weight: 400">Risk Management for Medical Devices and ISO 14971:2019 - Practitioner Training</li>
 	<li style="font-weight: 400">Safety for Electrical Medical Devices and IEC 60601</li>
 	<li style="font-weight: 400">Safety for Electrical Medical Devices and IEC 60601-1- Practitioner Training</li>
 	<li style="font-weight: 400">SAMD, IEC 62304 and IEC 82304-1</li>
 	<li style="font-weight: 400">SAMD, IEC 62304 and IEC 82304-1- Practitioner Training</li>
 	<li style="font-weight: 400">Software for Medical Devices and IEC 62304</li>
 	<li style="font-weight: 400">Software for Medical Devices and IEC 62304- Practitioner Training</li>
 	<li style="font-weight: 400">the Medical Device Regulation (EU) 2017/745</li>
 	<li style="font-weight: 400">Usability Engineering and IEC 62366-1</li>
 	<li style="font-weight: 400">Usability Engineering and IEC 62366-1- Practitioner Training</li>
 	<li style="font-weight: 400">Working in the Medical Device Industry</li>
</ul>

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Category: Education & Training Centres, Health & Safety, Healthcare & Pharmaceuticals, Medical Equipment

Description:

At Medical Device HQ, we specialise in delivering high-quality training solutions for professionals in the medical device industry. Trusted by individuals, companies, and regulatory bodies, we are dedicated to delivering excellence in every aspect of our training programs.

One thing that sets us apart is that our courses are created by members of the standardisation committees that authorise the ISO and IEC standards.

Our offerings include:

Pre-recorded online courses
Live virtual classroom sessions
Blended learning experiences combining an online course with interactive virtual or in-person classroom sessions
Customised, in-house training solutions tailored to the unique requirements of our clients

Covering topics such as:

Risk management
Quality management
Design controls
Project management
Software development
Usability engineering
Safety for medical devices
Clinical investigation
Medical Device Regulation compliance

Annually, we serve more than 3000 professionals globally, providing them with the knowledge and skills necessary to progress in their careers.

We have very happy customers, as reflected in our satisfaction rates:

96% of participants in our public classroom sessions would either recommend or highly recommend our courses
Our blended courses receive an average rating of 4.7 out of 5, while our instructors are rated 4.8 out of 5.

If you feel unsure about any area of bringing medical devices to the market, we encourage you to reach out. Whether you require information on a specific course or need assistance in a particular area, our team is here to support you.

Contact us today to discover how Medical Device HQ can help you achieve your professional goals and navigate the complexities of medical device product development with confidence.

Youtube: https://www.youtube.com/@MedicalDeviceHQ

Linkedin: https://www.linkedin.com/company/medicaldevicehq

Accredited Activities:

Advanced Risk Management for Medical Devices and ISO 14971:2019
Agile Medical Device Software Development
Clinical Investigation for Medical Devices and ISO 14155
Design Control for Medical Devices
Design Control for Medical Devices – Practitioner Training
How to Create a Medical Device Design and Development Plan
How to Create a Medical Device Risk Management Plan
ISO 13485 Internal Auditor Training
ISO 13485 Internal Auditor – Practitioner Training
Medical Device Requirements Engineering
Medical Device Requirements Engineering- Practitioner Training
PRRC – Person Responsible for Regulatory Compliance
Process Validation for Medical Devices
Process Validation for Medical Devices – Practitioner Training
Project Management for Product Development of Medical Devices
Project Management for Product Development of Medical Devices- Practitioner Training
Quality Management for Medical Devices and ISO 13485
Quality Management for Medical Devices and ISO 13485- Practitioner Training
Risk Management for Medical Devices and ISO 14971:2019
Risk Management for Medical Devices and ISO 14971:2019 – Practitioner Training
Safety for Electrical Medical Devices and IEC 60601
Safety for Electrical Medical Devices and IEC 60601-1- Practitioner Training
SAMD, IEC 62304 and IEC 82304-1
SAMD, IEC 62304 and IEC 82304-1- Practitioner Training
Software for Medical Devices and IEC 62304
Software for Medical Devices and IEC 62304- Practitioner Training
the Medical Device Regulation (EU) 2017/745
Usability Engineering and IEC 62366-1
Usability Engineering and IEC 62366-1- Practitioner Training
Working in the Medical Device Industry

Who Should Attend:

Our training courses are designed for professionals working within the medical device industry who seek to enhance their expertise and confidence in medical device product development.

Further Information:

https://medicaldevicehq.com/