Overview:

The Post Market Surveillance and Vigilance course is designed to help candidates 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.

Benefits:

Benefits of the Post Market Surveillance and Vigilance course:

• 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

Course details:

Course details of the Post Market Surveillance and Vigilance course:

Usual duration: One day

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