In Vitro Diagnostic Regulation (IVDR) programme

Nov
11
Date: 11th November 2020 -
17th November 2020
Time: 10:00 - 12:30
Duration: 5 morning sessions 2.5hrs each
Venue: Online Virtual Sessions 5 x 2.5hrs
Address: 11, 12, 13 & 16, 17 Nov.
Event details:

In Vitro Diagnostic Regulation (IVDR) programme

In Vitro Diagnostic Regulation (IVDR) programme

 For those Implementing the EU IVDR in their organisation, involved in writing technical files or upgrading quality systems for the EU IVDR along with Quality Engineers or Regulatory Affairs professionals.

Agenda:
1. Introduction to the In vitro diagnostic regulation
2. Classification & Conformity
3. Risk & General Safety Performance Requirements (GSPR’s)4. Performance Evaluation
5. Post Market Activities.

Benefits of the course:
Practical exercises to incite discussion and accelerate learning.
Provides an open forum to air concerns and ask questions.
Offers the opportunity to compare notes with industry peers.
A full set of course notes and guidance documents for post-course referral
Tutors with experience teaching Notified Bodies and Competent Authorities

 

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Delegate cancellation policy

Any cancellations received in writing up to two weeks prior to the event are refundable. All bookings are provisional until full payment is received.

Photography at events

There may be a photographer and videographer at the event and we may publish images from this event on our website(s) and on our social media accounts.

Price
Per delegate: €350.00
(plus VAT)
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