An NSF International Company M15 - IVD Regulations, Quality & Product Safety - IVD Clinical Data and Post Market Surveillance Plans
PrintPart of our Medical Devices Module 15
Dates:
Thursday 22 October 2025
Venue:
Manchester - Venue to be confirmed
Cost:
£735.00 excl VAT
Type: Medical Devices
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About this course
With changes to IVD regulation in Europe it will become more evident that IVD manufacturers will need to have robust PMS and clinical data. The methods of planning, conducting and documenting clinical data for IVDs are certainly different to general medical technologies; hence this course takes you through the best practices within this area. Full of examples, plans and solutions you will find this course of value if you are preparing for the changes
Who Should Attend
- Senior management
- Regulatory, quality, research, design, development,manufacturing, marketing managers and personnel
- Organizations preparing ‘own brand’ or ‘private label’ devices
- Distributors of IVDs
This is a new course offering for Medical Devices. For more information please call our team on +441142 541270. E-mail our training and education team at: [email protected]
