Essentials EU Medical Device Regulations

Learn the overview of European regulations governing medical devices.

Gain insight into the essential components of EU Medical Device Regulations (MDR).

Understand the reporting requirements and identification processes related to medical devices.

Acquire knowledge about the quality system involved in regulating medical devices.

Learn about compliance with EU MDR standards and guidelines.

Understand the importance of adhering to regulatory requirements for medical devices.

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Get a year-long access to the course.

No prerequisites; suitable for individuals from any academic background.

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Regulatory Affairs Specialist

Quality Assurance Manager

Compliance Officer

Product Safety Manager

Clinical Affairs Specialist

Medical Device Consultant

Module 01: Overview to European Regulations on Medical Devices

Module 02: Essential Components of EU MDR

Module 03: Reporting Requirements and Identification

Module 04: Quality System in Medical Device Regulation