English

This course is designed for professionals in the medical device industry, including engineers, quality control specialists, and regulatory affairs personnel, as well as students seeking to understand the Medical Device Regulation 2017/745 in simple terms. Learners will gain a clear understanding of the regulation's requirements, timelines, and compliance strategies necessary for market approval in the EU.

Medical Device Development

English (US)

Italian

Italiano

Understand regulations for medical devices in simple terms to gain market approval of a medical device in the EU.

medical-device-regulation-2017745-explained-in-simple-terms

Medical Device Regulation 2017/745 EU regulatory affairs.

Academic

Martin

Martin Conneely

This course is designed for junior regulatory affairs professionals, engineers with medical device experience, and anyone interested in navigating the US FDA regulations for medical devices. You will gain practical insights into the regulatory landscape and learn to effectively comply with FDA requirements. With real-world examples and exercises, you'll transform your understanding of how to bring a medical device to market in the US.

A practical course discussing the US FDA Medical Device regulations for real-world situations

practical-regulatory-affairs-2020-us-fda

Practical Regulatory Affairs 2020 - US FDA Medical Devices

Instructor

Pubudi

Pubudi Silva

Learn Medical Device Development today: find your Medical Device Development online course on Udemy

Medical Device Development Courses | Learn Online

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Beginner Favorites

This course is designed for professionals in the medical device industry, including engineers, quality control technicians, and regulatory affairs specialists, who wish to gain a clear understanding of the in vitro diagnostic medical device regulation 2017/746. Participants will transform their knowledge by learning the essential obligations and timelines necessary for compliance in the EU market. Whether you're a beginner or seeking to deepen your expertise, this course will empower you to navigate complex regulations with confidence.

Understand regulations for Invitro diagnostic medical devices in simple terms to gain EU market approval

ivdr-2017-746-regulatory-affairs

IVDR 2017 746 regulatory affairs: Learn EU compliance

This course is tailored for professionals in the medical device industry, including engineers, software developers, and project managers, whether they are beginners or seasoned experts. You will gain critical insights into the risk management process in line with ISO 14971:2019, empowering you to develop safe and effective medical devices efficiently. Unlock your potential as you learn to navigate the complexities of medical device development and compliance.

Become a Medical device development and risk management expert inline with ISO 14971:2019

master-medical-device-development-risk-management-course

ISO 14971 Medical Device Development & Risk Management

Founder of InnovEd Academy

Robert

Robert Ryan

This course is designed for individuals at all levels, including design engineers, production managers, and students interested in the medical device industry. You will gain a comprehensive understanding of the medical device design control process, enabling you to navigate compliance with ISO 13485, MDR, and CFR regulations. Prepare to transform your approach to medical device design and development, ensuring your products meet market approval standards.

Arabic

العربية

Understand Medical Device Design Control in simple terms to gain market approval. Compliance in the EU, US and Globally.

medical-device-design-development-control-iso-13485

Medical Device Design & Development Control. ISO 13485.

This course is perfect for anyone eager to understand the medical device software development process, including beginners. You will master critical standards like IEC 62304 and ISO 14971, transforming fragmented knowledge into a comprehensive understanding of safety-critical software principles and FDA regulations.

Master the IEC 62304 standard, FDA design controls, and risk management of medical device software

medical-device-software-process-blackbelt

Medical Device Software Process Blackbelt

Instructor at Udemy

Gerald

Gerald Rigdon

This course is designed for engineers and designers who are either new to the medical device industry or looking to stay updated on the European Union's Medical Device Regulation (MDR). Participants will gain a solid understanding of the requirements and obligations for designing and developing medical devices, ultimately enhancing their competence in the field. By the end of the series, you will feel empowered to navigate the MDR confidently and apply this knowledge to your projects.

English (UK)

An introduction to the EU's Medical Device Regulation (MDR) for those involved in developing medical devices

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Looking to advance your skills in Medical Device Development? We've got you.

Get everything you need to reach your goals in one convenient bundle.

Medical Device Regulation 2017/745 EU regulatory affairs.

Practical Regulatory Affairs 2020 - US FDA Medical Devices

Medical Device Regulation 2017/745 EU regulatory affairs.

Practical Regulatory Affairs 2020 - US FDA Medical Devices

Medical Device Development relates to Business Teaching & Academics

Medical Device Development Courses

Looking to advance your skills in Medical Device Development? We've got you.

Get everything you need to reach your goals in one convenient bundle.

Medical Device Regulation 2017/745 EU regulatory affairs.Understand regulations for medical devices in simple terms to gain market approval of a medical device in the EU.Rating: 4.5 out of 51654 reviews4 total hours53 lecturesAll Levels

Practical Regulatory Affairs 2020 - US FDA Medical DevicesA practical course discussing the US FDA Medical Device regulations for real-world situationsRating: 4.2 out of 51010 reviews1.5 total hours25 lecturesBeginner

Medical Device Regulation 2017/745 EU regulatory affairs.Understand regulations for medical devices in simple terms to gain market approval of a medical device in the EU.Rating: 4.5 out of 51654 reviews4 total hours53 lecturesAll Levels

Practical Regulatory Affairs 2020 - US FDA Medical DevicesA practical course discussing the US FDA Medical Device regulations for real-world situationsRating: 4.2 out of 51010 reviews1.5 total hours25 lecturesBeginner

Medical Device Development relates to BusinessTeaching & Academics

Medical Device Regulation 2017/745 EU regulatory affairs.

Practical Regulatory Affairs 2020 - US FDA Medical Devices

Medical Device Regulation 2017/745 EU regulatory affairs.

Practical Regulatory Affairs 2020 - US FDA Medical Devices

Medical Device Development relates to Business Teaching & Academics