NSF offers online training courses to learn about QMS and GMP in medical devices, ensuring that your product complies with international standards and…
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A one-day e-Learning course covering the differences between Medical Device Regulation EU 2017/745 compared to the Medical Device Directive.
This three-day seminar provides an introduction to the European medical device legislation. Find out more about the regulation and which products are covered.
Our Services ; EU IVD Medical Device Regulation – Introduction Training Course ; Introduction to EU Medical Devices Regulation Training Course ; ISO 13485:2016 - Medical Devices Quality Management Systems - Auditor Transition Training Course
Increase your knowledge of the updated EU Medical Devices Regulation with this online training course from SGS. Find out more.
Our ISO 13485 Medical Device training courses teach you how to boost quality, reduce risk, obtain CE approval and make excellence a habit. Enquire today.
By the end of this course, you will be able to: ; Recognize the regulatory background in Europe ; Identify the roles associated with the EU MDR ; Discuss the manufacturing requirements of the EU MDR
Online training on the key changes to the EU In Vitro Diagnostic (IVD) medical device regulation. Learn more about the updated Regulation for manufacturers and our certification course today.
Overview ; Access to good quality, affordable, and appropriate health products is indispensable to advance universal health coverage, address health emergencies, and promote healthier populations. Without medical devices, common medical procedures – from bandaging a sprained ankle, to diagnosing HIV/AIDS, implanting an artificial hip or any surgical intervention – would not be possible. Medical devices are used in many diverse settings, for example, by laypersons at home, by paramedical staf...