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A required part of conformity assessment and CE Marking is the need for Technical Documentation which includes the collation of supporting information about your IVD Device. Technical documentation is maintained throughout the product lifecycle. Learn how to assemble this and other types of required information so you can CE Mark your device in Europe.
This course will help you learn:
Expectations of Notified Bodies for technical file
Our on-demand courses allow learners access to knowledge-based content in real time, anywhere, and at anytime. Using established learning and interactive digital technology, on-line attendees are guided through the course content, at their own pace, providing opportunity to review, test knowledge and confirm understanding, as they progress through the course.
QA/Regulatory personnel involved in compiling technical documentation and design dossiers. Product design personnel and those in Research & Development for IVDs intended for the European market.
You should have a basic understanding of European IVD device regulations.
ติดต่อเราเพื่อดูว่าเราจะสามารถช่วยแนะนำคุณบนเส้นทางสู่ความสำเร็จในการดำเนินงานอย่างยั่งยืนได้อย่างไร