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DTSTART;VALUE=DATE:20250428
DTEND;VALUE=DATE:20250708
DTSTAMP:20260430T091000
CREATED:20250313T114215Z
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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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DTSTART;VALUE=DATE:20250519
DTEND;VALUE=DATE:20250729
DTSTAMP:20260430T091000
CREATED:20250428T085131Z
LAST-MODIFIED:20250428T090237Z
UID:13741-1747612800-1753747199@nobocap.eu
SUMMARY:Module 2: Generating Data for Technical Documentation (MDR)
DESCRIPTION:Master MDR Compliance with Our Online Postgraduate Course! \nNeed to navigate the complexities of the Medical Device Regulation (EU 2017/745)? This is your chance to gain the expertise needed to construct a Technical File and Clinical Evaluation Report – two critical pillars for regulatory compliance. \nModule 2: Generating Data for Technical Documentation (MDR) is a 10-week\, 100-hour online course designed for professionals looking to deepen their scientific and engineering knowledge in the Medical Devices sector. Upon completion\, you’ll earn a 5-credit EQF7 Certificate\, giving you advanced capabilities to meet the demands of the MDR. \n🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.🔹 Next! Go to the NoBoCap Courses section and register for Module 2 before May 9\, 2025. \nSave the date! Secure your spot early – places are limited. Don’t miss this opportunity to boost your expertise in MDR compliance! \nModule 2 starts on May 19\, 2025. \nClick here: https://portal.nobocap.eu and take the next step toward advancing your MedTech career!
URL:https://nobocap.eu/event/module-2-generating-data-for-technical-documentation-mdr/
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