Online training on the basics of the IVDR (EU) 2017/746 requirements
Are you aware of the impact of IVDR on your business? The new EU IVDR will bring several changes and affects the IVD economic operators in the entire supply chain, like manufacturers, distributors, importers and suppliers. To support operators to comply with the new IVDR requirements, Labquality will offer an online training course consisting of six sessions. The Labquality training course helps your company understand the key changes and their impact on your business.
The training will provide participants with an overview of the critical changes in relation to new EU IVDR. You can participate in the complete training course or pick the most suitable sessions for you. Sign up for the complete training course here or use the button below. If you want to participate in the individual sessions you can choose the ones you are interested in from the links under the session descriptions.
If you order the complete course by 26 September 2022, you will get a -25% discount using the coupon code IVDR2021.
Contact our Training firstname.lastname@example.org
+358 9 8566 8200
Receive updates on our training calendar by subscribing our notifications:
Topics of this session
Mari KukkonenQuality and Development Manager
Anja KontioQuality and Regulatory Affairs Manager
Target groupOur training is intended for quality and regulatory affairs managers and specialists, IVD designers, project managers, marketing managers, operations managers, and other responsible persons working in the IVD industry, and for other economic operators in the supply chain who need to understand at least the basics of the IVDR. Participants will receive a course certificate via email after the course. All attendees are granted free and unlimited access to Entries, the Digital Regulatory Runways for the duration of a full year.
After this session, youThe participants will understand the impact of the new In-Vitro Diagnostic Regulation (IVDR), the most relevant changes compared to the directive, and how the IVDR will impact medical devices already on the market as well as new medical devices.
Billing and cancellation policy
Participation in the training can be cancelled two weeks (14 days) before the event free of charge. For cancellations made after this, we will charge 50% of the participation fee, except for cancellations made one week before the event, we will charge a 100% participation fee.
Cancellations are always made in writing to: email@example.com.
The participating organization may, if it wishes, change the participant free of charge by notifying it in writing before the event to: firstname.lastname@example.org. The participation fee will be invoiced immediately after the event. The training session will be confirmed to the participant by e-mail about a week before the event. Labquality reserves the right to cancel the training session due to a small number of participants.