Updated post-market surveillance rules for medical devices in the UK: differences from the EU regulations
There is greater clarity on timings, in that the PMSR must be: (i) produced within three years of the device […]
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Post-marketing safety of immunomodulatory drugs in multiple myeloma: A pharmacovigilance investigation based on ..
Objective: In recent years, the emergence of immunomodulatory drugs (IMiDs) has significantly improved clinical outcomes in patients with multiple myeloma…
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Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostic
Post-market surveillance is a set of activities conducted by manufacturers, to collect and evaluate experience gained from medical devices…
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Post-Market Surveillance Resource Center
The MTI Post-Market Surveillance Resource Center provides current news and information specific to maintaining medical device post market product quality…
Post-Market Surveillance Resource Center Read Post »