Course Description
Essentials of European Medical Device Regulations (EU MDR) – 2017/745
Alison
In this free online course learn about the key aspects of the European Medical Device Regulations (EU MDR) – 2017/745. This free online course explains the essentials of European Medical Device Regulations (EU MDR) – 2017/745. The course provides a way for learners to study the complex and detailed regulations, including the improvements in the EU MDR, the technical files elements, post-market responsibilities, increased requirements related to market actors etc. This course will be interest to all professionals working in the medical devices’ industry.
Online Course
| Course Code | 2218 |
| College Name | Alison |
| Course Category | Business, Health Care, Healthcare Management, Healthcare Management |
| Course Type | Online Learning |
| Course Qualification | CPD Certificate |
| Course Location | Online Course |
| Delivery mode | |
| Course Fee | Free |
| Course Duration | 1.5-3 hours |
| Entry Requirements | Like all courses on the Alison Free Learning platform this is a free, CPD-accredited course. A Graduate can choose to buy a certificate or diploma upon successful completion of a course, but this is not required or necessary. At Alison we believe that free education, more than anything, has the power to break through boundaries and transform lives. Alison is the world’s largest free online empowerment platform for education and skills training, offering over 5000 CPD accredited courses and a range of impactful career development tools. It is a for-profit social enterprise dedicated to making it possible for anyone, to study anything, anywhere, at any time, for free online, at any subject level. Through our mission, we are a catalyst for positive social change, creating opportunity, prosperity, and equality for everyone. |
| Career Path | In This Free Course, You Will Learn How To • Explain the three directives on medical devices: IVDD, MDD & AIMDD • Discuss the transformation of old EU directives into new regulations, and their relationships • Summarize the important improvements with the new EU MDR • Differentiate the different classes of medical devices and the criteria for classification • List the 22 rules of product classification for a medical device • Interpret the route to market for medical devices in Europe • Evaluate the roles of different economic operators in EU • Describe the applications and requirements of EU-UDI • Specify the requirements on EUDAMED in EU MDR |
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