Capturing customer feedback and managing risk is crucial to the success and compliance of all medical devices. Achieve both with our Medical Device Post Market Surveillance and Vigilance Training Course – helping you gather data to secure continued compliance with the Food and Drug Administration (FDA) and Medical Device Directives (MDD).
Our one day course will give you the tools to carry out successful post market surveillance. Explore ways to capture feedback, record market trends and understand how regularly monitoring data can improve quality and safety controls. You will also learn to handle complaints, clinical follow up, quality and risk management, and MDD and FDA compliance.
“The course was delivered in a clear manner and easily understood.”
Identifying and using the right information will keep you one step ahead. Complete the course and you can confidently carry out effective post market surveillance and increase market access.
£740 + VAT
1 day
Includes refreshments, lunch and course notes.
Who should attend?
- Regulatory and design and development professionals
- Clinical affairs specialists and those handling complaints
- Quality managers and those working in sales or marketing.
Call our training advisors now
+44 (0)845 086 9000
training@bsigroup.com