Post-market Surveillance and Vigilance Training Course

BSI’s “Post-market Surveillance and Vigilance” 1 day course is designed to help you identify the requirements of the European medical device directives (90/385/EEC, 93/42/EEC, 98/79/EC), standards and guidance documents to enable effective implementation of a post market surveillance system.

Who should attend?

  • Regulatory professionals
  • Quality managers
  • Clinical affairs specialists
  • Complaint handling specialists
  • Design and development professionals
  • Medical Device Sales & marketing.

What will I learn?

On completion of this training, participants will be able to:

  • Confirm the PMS regulatory requirements of the directives required for the particular class of product
  • Create a procedure that includes both proactive and reactive sources of information
  • Implement cost effective and targeted post-market clinical follow-up using various tools and techniques
  • Recognise when a complaint needs to be reported as an incident.

What is included?

  • Course information 
  • Dinner
  • Coffee break 

You’ll be awarded an internationally recognized BSI Training Academy certificate.