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
  • Lunch
  • Refreshments

 

In-house training

If you have a group of people to train and a single location that is practical, an expert tutor can deliver training at your premises. Want to know more?

 

Request an in-house training quote >


COVID-19: Important information on classroom-based training courses

BSI is closely monitoring UK Government Advice regarding the safety of classroom-based training courses. In the event of a classroom-based course being deemed unsafe, your training booking will be automatically transferred to online delivery using our highly-interactive virtual classroom - Connected Learning Live.

If you have any questions regarding your booking, please contact training@bsigroup.com or call +44 345 086 9000.


Booking a course delivered via Connected Learning Live?

Take advantage of our exclusive offers, only available in July and August 2020*

Book a July or August Connected Learning Live course date and you’re entitled to unlock one of the following benefits:

  • Option 1: Get 50% off a second delegate booking fee
    Offer applicable to public courses delivered via Connected Learning Live in July and August 2020 only. Second delegate must attend the same course date
  • Option 2: Save £500 on a BSI Diploma in Quality Management
    Offer applicable to delegates that have booked a public course delivered via Connected Learning Live in July and August 2020 only

Contact our training team today to find out more and book your place. Call +44 345 086 9000 or email training@bsigroup.com

*Terms and conditions: Applies to all public BSI UK training courses, taking place in July and August 2020 via Connected Learning Live only. Call our training team on +44 345 086 9000 or email training@bsigroup.com for more information. Second delegate must attend the same course date as the first delegate. Moves, changes and cancellations are not permitted. Payment required or invoice issued at the time of bookings. This offer does not apply to BSI re-sellers or Cybersecurity and BRCGS courses. Offer is for new BSI UK training bookings only. Offer is not to be used in conjunction with any other offer. Offer subject to availability of training courses. Bookings are non-transferable. All other terms and conditions for training courses apply.