Eu Medical Device Regulation Training

Its requirements refer to the european commission as well as medical device manufacturers notified bodies and member state competent authorities.

Eu medical device regulation training.

The european regulations on medical devices including active implantable medical devices aimd eu mdr 2017 745 was published on may 5th 2017 and entered into force on may 25th 2017 with may 26th 2020 as its application date there is not a lot of time left for medical device companies to get up to speed. All medical devices and identified devices without a medical purpose will need to undergo a conformity assessment procedure based on the new mdr requirements in order to place devices on the. The adoption in april 2017 of regulation eu 2017 745 on medical devices mdr and regulation eu 2017 746 on in vitro diagnostic devices ivdr changed the european legal framework for medical devices introducing new responsibilities for ema and for national competent authorities. The new european union medical device regulation mdr 2017 745 represents a considerable change from the directives it is replacing.

Medical devices training nsf international provides regulatory and quality medical devices training courses and professional qualifications. Device manufacturers who conduct business in the eu must start their transition now in order to meet the may 26 2021 transition deadline. Mdr training resources regulation 745 2017 on medical devices. Learn eu mdr 2017 745 online for free.

I offer you a free medical device regulation training course with a quiz and certificate of completion. Published as regulation eu 2017 745 it covers medical devices and active implantable medical devices. Main changes and timeline to implementation regulation 745 2017 on medical devices. This course introduces you to the key changes from the european medical device directive mdd to the new european medical device regulation mdr.

We have worked with more than 90 of the leading medical device companies to elevate the skills and competence of their employees. On site eu mdr training with experienced medical device consultants our mdr training is an excellent value for companies training three or more employees at a time. We can assist in many ways from 300 sessions of public ra qa classes to on site group training and coaching. Nsf s training courses are highly interactive and based on real scenarios helping you meet international requirements throughout the product lifecycle.

The training is conducted at your facility by senior regulatory consultants who spend most of their time working with clients on mdr compliance not jumping from city to city. Obligations of the economic operators from eudamed registration to responsible person regulation 745 2017 on medical devices. Unique device identification regulation 745 2017 on medical devices.