M15 - IVD Regulations, Quality & Product Safety - Planning For the Revision of the IVD Directive 98/79/EEC

About this course

A one day course aimed towards enabling people involved in IVD regulatory to understand the impact of the regulation and ensure an appropriate plan is in place to address the new requirements in 2015. This course will be particularly appealing to those personnel responsible for the commercial planning of products set to fall under the new IVD Directive.

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]

Course outline

Venue

Manchester - Venue to be confirmed

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Tutors

The tutor for this course is as follows:

• 

  Sarah Couch
  Medical Devices Consultant
  

  • [email protected]
  • +44 (0) 1143 600868

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