Medical Device HQ AB

CPD Standards Office Provider Number: 50513

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Accredited Activities

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

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

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/