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Medical Devices and IVD Training

Artixio provides real-world, current, experience driven regulatory, quality, safety, product design training courses and professional certification. Artixio’s trainings and programs help you continuously up-skill and stay ahead of new developments in industry throughout your career journey. Our programs are designed to help individuals right from their academic to professional journey.

 

Artixio’s training programs are based on our team’s global experience working with different health authorities, notified bodies, professional institutions and leading experts in medical devices and IVD industry.

Medical Devices Regulatory Training is a comprehensive training program that provides you with the knowledge and skills you need to comply with the latest medical device regulations. The program covers a wide range of topics, including:

  • The Medical Device Regulation (MDR)

  • The In Vitro Diagnostic Medical Device Regulation (IVDR)

  • ISO 13485:2016

  • Risk management

  • Clinical evaluation

  • Post-market surveillance

  • UDI

  • Notified bodies

 

The programs are delivered by experienced regulatory experts who will help you understand the regulations and how to apply them to your specific products. You will also have the opportunity to network with other medical device professionals and learn from their experiences.

Benefits of Medical Devices Regulatory Training from Artixio

There are many benefits to completing Medical Devices Regulatory Training, including:

  • Increased compliance with medical device regulations

  • Reduced risk of product recalls

  • Improved market access

  • Enhanced brand reputation

  • Increased knowledge and skills

  • Networking opportunities

Who Should Attend Medical Devices Regulatory Training

Medical Devices Regulatory Training is ideal for anyone involved in the development, manufacture, or marketing of medical devices. This includes:

  • Product managers

  • Quality engineers

  • Regulatory affairs professionals

  • Sales and marketing professionals

  • Engineers

  • Technicians

 

Schedule and Format

Medical Devices Regulatory Training is available in a variety of formats, including:

  • In-person classroom training

  • Virtual online training

  • Self-paced e-learning

 

The length of the program varies depending on the format you choose. In-person classroom training typically lasts for 2-5 days, while virtual online training and self-paced e-learning can be completed in as little as 1-2 weeks.

On-Site Training (On-Demand)

Advanced Training on Medical Devices Compliance 

The program aims to dive deep in to each topic with Real-World examples and to help professionals from medical devices industry to gain insights and hands on experience on solving compliance related problems in Medical Devices industry.

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Online Trainings

No available programs
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