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DTSTART;TZID=Europe/Paris:20260528T090000
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DTSTAMP:20260501T193546
CREATED:20260308T165211Z
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UID:8289-1779958800-1779985800@www.team-nb.org
SUMMARY:MDR Clinical Training for Manufacturers
DESCRIPTION:Registration Fees & Deadlines\n600 € for SMEs – Priority for SMEs registration (25 places reserved) until March 27th\n1200 € for organisation \nYou can register until April 28th \n\nEvent Summary\nClinical Evaluation Review Training for Manufacturers: lesson learnt and the do’s and don’t’s based on non-conformities examples.\n\nThis training is directed towards manufacturers/participants who already have experience in creating CER and/or are involved in CE submission. Therefore\, the training will focus more on real cases examples and less on introduction or citing regulations.  \nThe topics are presented by MDR experts of designated notified bodies.\n\nThe content was elaborated by MDR experts of 3 notified bodies\, namely BSI\, CeCertiso\, Dekra.\n\nThis training is intended for participants who are members of a manufacturer’s clinical team and have experience in creating CERs and/or are involved in CE submission. Therefore\, can you consider this exper-tise for registrations.  \n  \n\nPROGRAM\n\n\n\n09.00 – 09.30\n\nWelcome and logistic information\n\n\n\n\n\n\n\n09.30 – 10.45\n\nClinical evaluation routes\n\n\n\n \nÁgnes Horvath\, CE Certiso\n\n\n\n\n\n\n\n10.45 – 11.00\n \nBreak\n\n\n\n\n\n\n\n11.00 – 12.30\n\nHow to build sufficient clinical evidence?\n\n\n\n \nNunung Nur Rahmah\, Dekra NL\n\n\n\n\n\n\n\n12:30 – 13:30\n \nLunch\n\n\n\n\n\n\n\n13.30 – 14.45\n \nPost market surveillance and PMCF\n\n\n\n\nBreda Kearney\, BSI\n\n\n\n\n\n\n\n14.45 – 15.00\n \nBreak\n\n\n\n\n\n\n\n15.00 – 16.00\n \nQ&A session\n\n\n\n\n\n\n\n16.00 – 16.30\n \nClosing session\n\n\n\n\n\n\n\n\n\n\n\n\n\n\nREGISTRATION
URL:https://www.team-nb.org/event/mdr-clinical-training-for-manufacturers-3/
LOCATION:Remotely
CATEGORIES:Public
ATTACH;FMTTYPE=image/jpeg:https://www.team-nb.org/wp-content/uploads/2026/04/MDR-CLINICAL-TRAINING.jpg
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