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EC Medical Devices Vigilance System and Post Marketing Surveillance Training Course
26th January 2021 @ 9:00 am - 27th January 2021 @ 5:00 pm

Location: Online webinar
Description: This seminar will give you practical advice on how to comply with the EU vigilance and post-market surveillance requirements. It will highlight manufacturers’ legal obligations and the risks associated with litigation, as well as providing essential guidance on how to report incidents in order to remain compliant. You will also gain practical advice and guidance on how to handle adverse event reporting during medical device clinical studies.
Organiser: Management Forum
Contact: +44 (0)20 7749 4730

