Medical Device Regulation Transition Timeline (MDR 2017/745)

Medical Device Regulation Training: Learn about the hard and the soft transition for your Medical Devices within the MDR 2017/745 and IVDR 2017/746. I will show you how you should strategies the transition of your portfolio. Medical Device Regulation should be implemented for manufacturers in the Medical Device Industry that are selling products to Europe. If you are located in Europe or outside of Europe, you'll have to comply with this regulation. If you want to continue to sell Medical Devices Products approved under MDD until May 2025, then you'll need to place them on the market. What does mean "Placing on the market". I will let you know with another video. I hope this video was helpful to you. -------------------------------------------------------------------------------------------- Links from the Video Article "Medical Device Regulation Transition Timeline": https://easymedicaldevice.com/mdr-tra... Mini-Course MDR 2017/745: https://easymedicaldevice.com/mdr Text MDR 2017/745: https://easymedicaldevice.com/resourc... ------------------------------------------------------------------------------------------- Social Media to follow Linkedin:   / melazzouzi   Twitter:   / elazzouzim   Pinterest:   / easymedicaldevice   Instagram:   / easymedicaldevice   ------------------------------------------------------------------------------------------ #medtech #medicaldevice #compliance