IVD Directive to IVD Regulation Transition training course

Niveau Gespecialiseerde vaktraining Duur 1 day

Beschikbaar om te boeken: Virtuele training geleid door instructeur €1220 View dates, locations and prices

There are significant changes in the European legislation applicable to IVDs. The IVD Regulation (EU 2017/746) has replaced the IVD Directive (98/79/EC), and will impose new requirements on manufacturers and other Economic Operators.

This long awaited text brings a number of significant changes to the regulatory requirements for IVD manufacturers, addressing the challenges posed by the IVD Directive. The changes include a new rule-based classification system, increased scrutiny of technical documentation, and improved traceability of devices through the supply chain.

Our one day training course has been designed to introduce IVD manufacturers and other Economic Operators in the supply chain to the key changes to requirements for CE marking following the publication of the new IVD Regulation (IVDR).

Online training courses: Connected Learning Live
You can attend this training course classroom based and online. Do you prefer the convenience of an online training course? View here for the available dates or read more about Connected Learning Live.

Combination discount

Attending several medical device courses is associated with special combination discount.

1. Transition or Requirements IVD - IVDR

2. Implementing CE Marking IVDR

Combination training 1 + 2

In-house training courses
For more information about combination of courses or in-house training courses, please contact our Training Advisors via +31 20 346 0780 or send an email to training.nl@bsigroup.com

For further information regarding reduced rates at the hotel where the training is being conducted please contact us.

- Requirements and impacts of new IVD Regulation
- Key aspects of the transition - from Directive to Regulation
- Changes to responsibilities of Economic Operators
- Significant changes introduce by the new IVD Regulation
- Revised scope, risk-based classification, and conformity assessment
- Revised clinical expectations
- Managing the transition
- New expectations for post-market activities
- Technical documentation for compliance
- Medical device manufacturers, especially if your role is in:
• Regulatory Affairs
• Design and Development
• Clinical Affairs Specialists
• Quality Management
• Quality Assurance
- Authorized Representatives
- Economic Operators, including importers and distributors
- Consultants
- It's a 1-day course
- The training and materials will be provided in English
- Lunch and drinks are included for the classroom training

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