M3 - CE & Global Clinical Requirements - Post Market Clinical Follow Up for Medical Devices (QP)

About this course

Within the European medical device directives there are specific requirements for obtaining post-market data relating to the clinical performance of your product utilizing a post market clinical follow-up plan. This course presents the requirements for PMCF and will enable you to understand the requirements and apply them to your internal procedures.

Who Should Attend

Development, regulatory and clinical personnel involved in the formulation of clinical investigations, evaluations and post market clinical follow-up of medical devices. The medical devices requirements are placing a major emphasis upon clinical data requirements for devices therefore programme managers, marketing and senior managers will also benefit from this module in that they will be able to understand the clinical requirements necessary for their devices and plan an appropriate commercialization strategy.

Course outline

This is a new course offering for Medical Devices and part of our Qualified Person programme for Medical Devices. For more information please call our team on +441142 541270. E-mail our training and education team at: [email protected]

Venue

Manchester - Venue to be confirmed

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Tutors

We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.

Our experts for this course are:

• Rikke Arendt Christiansen

• 

  Yvonne Middlefell
  Medical Devices, Executive Director Regulatory Affairs
  

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

What you've said

This is a new course for NSF-DBA and we will soon be able to provide you with feedback from our Medical Device programme.