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X-WR-CALDESC:Events for NoBoCap
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DTSTART:20250101T000000
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DTSTART;VALUE=DATE:20250210
DTEND;VALUE=DATE:20250422
DTSTAMP:20260430T121149
CREATED:20250130T085110Z
LAST-MODIFIED:20250130T085110Z
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SUMMARY:Module 1: Implementing Regulatory Requirements for Medical Devices
DESCRIPTION:Unlock the skills you need to become an expert in Medical Devices Regulation (MDR) with our online postgraduate-level courses! \nWhether you’re aiming to work in medical device manufacturing\, auditing\, or product assessment\, this module is your first step toward achieving MDR compliance. It’s a 10-week\, 100% online course that offers 5 CPD credits and a Postgraduate Certificate accredited by theUniversity of Medicine\, Pharmacy\, Sciences and Technology of Târgu Mureş. \nFirst Step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu\, then find Post Graduate Courses section and register for the Module 1. \nDon’t miss this opportunity! Secure your spot today—places are limited. Register now before it’s too late! \nModule 1 starts in February 10\, 2025. \nClick here on https://portal.nobocap.eu and take the next step toward enhancing your MedTech career!
URL:https://nobocap.eu/event/module-1-implementing-regulatory-requirements-for-medical-devices/
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DTSTART;VALUE=DATE:20250428
DTEND;VALUE=DATE:20250708
DTSTAMP:20260430T121149
CREATED:20250313T114215Z
LAST-MODIFIED:20250403T151033Z
UID:13691-1745798400-1751932799@nobocap.eu
SUMMARY:Module 3: Generating Data for Technical Documentation (IVDR)
DESCRIPTION:Master the Art of IVDR Compliance with Our Online Postgraduate Course! \nNeed to navigate the complexities of the In Vitro Diagnostic Devices Regulation? This is your chance to gain the expertise needed to construct a Technical File and Performance Evaluation Report – two essential elements for regulatory compliance. \nModule 3: Generating Data for Technical Documentation (IVDR) is a 10-week\, 100-hour online course designed for professionals looking to build on their scientific and engineering knowledge in the IVD sector. Upon completion\, you’ll earn a 5-credit EQF7 Certificate\, equipping you with advanced regulatory skills. \n🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.🔹 Then\, go to the NoBoCap Courses section and register for Module 3. \nSave the date! Secure your spot early – places are limited. Don’t miss this opportunity to advance your career in IVDR compliance! \nModule 3 starts on April 28\, 2025. \nClick here on https://portal.nobocap.eu and take the next step toward enhancing your MedTech career!
URL:https://nobocap.eu/event/module-3-generating-data-for-technical-documentation-ivdr/
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