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Module 3: Generating Data for Technical Documentation (IVDR)

April 28 - July 7

  • « NoBoCap Community Online Webinar
  • C-level Management Training »

Master the Art of IVDR Compliance with Our Online Postgraduate Course!

Need 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.

Module 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.

🔹 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.

Save the date! Secure your spot early – places are limited. Don’t miss this opportunity to advance your career in IVDR compliance!

Module 3 starts on April 28, 2025.

Click here on https://portal.nobocap.eu and take the next step toward enhancing your MedTech career!

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Details

Start:
April 28
End:
July 7
Website:
https://portal.nobocap.eu/

Venue

ZOOM
  • « NoBoCap Community Online Webinar
  • C-level Management Training »

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Contact information

nobocap@rohealth.ro

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  • Home
  • About
    • About NoBoCap
    • WPS
  • Community
    • NoBoCap Community Summit 2024 program
    • About the community
    • What is Offered
    • Community Members & Partners
    • Repository of EU Regulatory Support
  • News
  • Events
  • Surveys
  • Public documents
  • Contact us
  • Join NoBoCap Environment

Email: nobocap@rohealth.ro