Implementation of the In Vitro Diagnostic Device Regulation for CE Marking

On-demand eLearning course

Implementation of the In Vitro Diagnostic Device Regulation (IVDR) for CE Marking On-demand eLearning course

等級標準建置期間 1.5 days

可報名: 線上隨選課程 NT$12000 Book your place

The In Vitro Diagnostic Devices Regulation (IVDR 2017/746) is the legislation detailing the requirements which manufacturers have to meet to place in vitro diagnostic devices on the market in the European Union. The Regulation contains detailed requirements that need to be implemented, and will affect all IVD manufacturers, importers, distributors and EU Representatives.

The IVDR focuses on devices to be safe and effective, emphasizing pre-market requirements, conformity assessment, post-market-surveillance (PMS), and traceability. This course aims to offer guidance on implementation of the requirements stipulated in the IVDR into your business.

BSI’s on-demand courses are market-leading and available 24/7. Developed by top subject matter experts, they contain the same high-quality content you will find in our tutor-led training, but with the added benefit of being able to learn at your own pace and at any time.

How will I benefit?

This course will help you:

Take the necessary steps for your organization to meet the IVDR requirement
Implement the requirements of the European In Vitro Diagnostics Devices Regulation
Execute robust and compliant performance evaluation and post market follow up studies
Guide and support other people and partner organizations affected by IVDR

By the end of the course delegates will be able to:
- Develop a strategy for regulatory compliance as stipulated by IVDR · Recognise the roles and responsibilities of Economic Operators (legal manufacturer, Authorised representative, Importer and Distributor) and other Key Players (Notified Body, Competent Authority, significant subcontractors) under the IVDR
- Explore the role of the Notified Body
- Implement requirements concerning the following steps for Placing on the Market: o Scope and applicability of IVDR
  
  EU risk classification criteria for IVDs to determine “Risk Class”
  
  General Safety and Performance Requirements as the basis for CE Marking, including the use of standards and Common Specifications
  
  Risk Management and related planning o Technical documentation
  
  Labelling and UDI
  
  Conformity assessment routes and their application based on risk-class
  
  Self-certification, CE-certification by Notified bodies
  
  Other key Regulations and Directives
  
  EUDAMED and registration
- Plan post-market activities required by IVDR with respect to:
  
  Post-Market Surveillance and post-market Follow-Up
  
  Periodic reports, Vigilance, ad-hoc Reporting
  
  Risk management throughout the product lifecycle
  
  Involvement of authorities, scrutiny
  
  Notification of significant changes
- Impart knowledge concerning IVDR requirements into your organization, e.g. in projects for CE-marking
The course is especially suitable for:
- RA, QM, and QA professionals who will be implementing the IVDR within their organisations
- Personnel concerned with certification or active in projects for CE-marking, including R&D scientists, production personnel, project management.
- Staff in contact with IVD Device manufacturers at companies which are partners to manufacturer, e.g. as subcontractor, crucial supplier, OEM, Authorized representative, importer, distributor, auditee
This is an online, interactive on-demand course.

Courses are available 24/7 and you can learn at any time and from any place that suits you – you just need an internet connection.

You can learn as fast or as slowly as you want to. You can also take breaks at any time in the course and pick up where you left off when you are ready to continue.

During the access period, you can go back and repeat parts or all the course to refresh and reinforce what you have learned.

The course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning.
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
Convenient - courses are available 24/7 and you can learn at any time and from any place that suits you – you just need an internet connection

Learning pace - You can learn as fast or as slowly as you want to. You can also take breaks at any time in the course and pick up where you left off when you are ready to continue

Information retention - During the access period, you can go back and repeat parts or all the course to refresh and reinforce what you have learned

High-quality materials - Developed by top subject matter experts, course content is both detailed and engaging, with explanations, activities, and knowledge checks to enhance your learning

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