Implementation of the In Vitro Diagnostic Device Regulation for CE Marking Training Course

To help implement the requirements of the European In Vitro Diagnostic Device Regulation (IVDR 2017/746) to obtain and maintain the CE mark for your product. Gain confidence with the IVD classification rules and the conformity assessment routes. Learn the importance of the General Safety and Performance Requirements in product development, and of scientifically robust performance evaluation and clinical evidence.

Explore the role of risk management during product development and in post market follow up. Develop an understanding of the interface and interaction with Notified Bodies, economic operators (importers, distributors, EU Representatives) and subcontractors/suppliers, according to their obligations under the IVDR.

Who should attend?

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

We also offer an equivalent training course for implementation of the Medical Device Regulation for CE Marking.

What will I learn?

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:
    • 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
    • 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

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 organisations affected by IVDR

What's included?

  • You will gain 8 CPD points on completing the course
  • Training course notes

 


Classroom-based training: Ready when you are

When you’re ready for face-to-face training again, we’re ready to welcome you.

As we all adjust to greater freedom around travel and meetings, we want to reassure you that our training team has worked with venues and tutors to enhance measures to keep you safe. Our carefully selected training venues continue to operate social distancing procedures, with readily available sanitizer stations at high-touch points throughout the venue. Rigorous deep cleaning procedures continue, providing you with peace of mind during your time at the venue.

If you have any questions regarding your booking of a classroom-based training course, please contact training@bsigroup.com or call +44 345 086 9000.