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An opportunity for BSI to share best practices on compiling and submitting Periodic Safety Update Report (PSURs) for Notified Body evaluation.
This insightful webinar will be beneficial for those with medical device Post-market Surveillance responsibilities under EU MDR.
The role of MDCG 2022-21 guidance on PSUR for manufacturers.
Providing justifications and analysis.
The data collection period & stratification of data.
Change notification via the PSUR.
Post Market Surveillance Regulatory Lead, BSI
Technical Team Manager - Orthopaedics and Dental, BSI
Clinical Regulatory Lead, BSI
Reach out and see how we can help guide you on your path to sustainable operational success.