CarrièresEspace presseCOVID-19
  1. Home
  2. Services
  3. Customer Services
  4. UpSkill Services
  5. IVDR Training

IVDR Training

Book training now to master your transition to IVDR

Time is running out. The new European Union In Vitro Diagnostics Regulation (EU IVDR)1 will come into force on May 26, 2022, for products such as reagents, assays, consumables, systems, and software. The production of these devices must comply with the new EU IVDR rules prior to the date of application of the EU IVDR; otherwise they will be banned from the European market.

The complexity of the new EU IVDR makes this challenging for both manufacturers and healthcare providers. That’s why we developed dedicated modular online training to help you get you up to speed with the EU IVDR reliably – as fast and easily as possible.

Our new EU IVDR-specific training program includes both virtual and self-study content for manufacturers and laboratory professionals. Three different training modules help you transition to the new EU IVDR, understand the requirements, and gain a better understanding of how to apply them in your own organizations.

IVDR Overview

IVDR Essentials

IVDR Advanced

Basic Regulatory Training, which includes general information on the changeover to
the new directive as well as timelines, requirements, and overall structure of the EU IVDR

✓

✓

✓

Laboratory Training, which specifically addresses the specimen produced or utilized by
clinical laboratories
or
Manufacturer Training, which specifically addresses how to provide IVDs on the market
for IVD manufacturers and their organizations

-

✓

✓

Expert Live Q&A Session, which provides the opportunity to interact, network,
and discuss your organizations’ challenges

-

-

✓

Participants

max. 25 

max. 25 

max. 25 

Virtual course

2.5 hours

4.5 hours

9 hours

Price

€250 pp plus VAT

€600 pp plus VAT

€1,000 pp plus VAT

IVDR Training Subvisual 1

IVDR Overview Training

Provides the basics for all EU IVDR actors

This training includes

  • Basic regulatory training
  • General information on the changeover to the new directive
  • Timelines, requirements and overall structure of the IVDR
This training module is delivered as a 2.5 hour virtual course led by an IVDR expert.

Price: €250€ pp plus VAT

All trainings are limited to a maximum of 25 participants.

Once registered, a representative from Siemens Healthineers will contact you for details.

IVDR Training Subvisual 2

IVDR Essentials Training

Offers a deep dive for laboratory professionals & manufacturers

This training includes
  • IVDR Overview Training Materials
plus one of the below modules
  • Laboratory Training, which specifically addresses the specimen produced or utilized by clinical laboratories
    (This course is suitable for all those involved with creating and applying IVDs in the laboratory environment or at point of care.)
or
  • Manufacturer Training, which specifically addresses how to provide IVDs on the market for IVD manufacturers and their organizations

IVDR Overview Training Materials are provided for download and self-study.
Laboratory / Manufacturer Training is delivered as a 4.5 hour virtual course led by an IVDR expert.

Price: €600 pp plus VAT

All trainings are limited to a maximum of 25 participants.

Once registered, a representative from Siemens Healthineers will contact you for details.

IVDR Training Subvisual 3

IVDR Advanced Training

Addresses your individual challenges as laboratory professionals & manufacturers

This training includes

  • IVDR Overview Training
plus
  • IVDR Essentials Training
plus
  • Expert Live Q&A Session, which provides the opportunity to interact, network, and discuss your organizations’ challenges

IVDR Overview Training is delivered as a 2.5 hour virtual course led by an IVDR expert.
IVDR Essentials Training is delivered as a 4.5 hour virtual course led by an IVDR expert.
Expert Q&A virtual sessions are 2 hours.

Price: €1,000€ pp plus VAT

All trainings are limited to a maximum of 25 participants.

Once registered, a representative from Siemens Healthineers will contact you for details.

Why book training with us?

As a manufacturer, we have been involved in the application of the EU IVDR from the very beginning. Combined with our experience as a certified training provider, our experts can help you understand the new requirements. We will share our knowledge in online trainings to support your transition and guide you through the implementation process. 

The products/features and/or service offerings (here mentioned) are not commercially available in all countries and/or for all modalities. If the services are not marketed in countries due to regulatory or other reasons, the service offering cannot be guaranteed. Please contact your local Siemens Healthineers organization for further details.

1

REGULATION (EU) 2017/746 OF THE EUROPEAN PARLIAMENT AND COUNCIL of April 5, 2017 on in-vitro diagnostic medical devices