Product and Medication-Use Error Briefings
Leverage exclusive error data to proactively address product safety risks.
Tackle product safety risks with exclusive error data and targeted research
Manufacturers face ongoing challenges in detecting and addressing safety risks, with thousands of errors reported annually across multiple databases. Without timely insights, manufacturers risk overlooking critical safety issues, which can result in preventable harm, regulatory noncompliance, and damage to their brand reputation.
Exclusive insights from critical error databases
Med Safety Board (MSB) partners with manufacturers to enhance product safety by leveraging exclusive access to key error databases, including ISMP Medication National Error Reporting Program (MERP), National Vaccine Errors Reporting Program (VERP), and the National Consumer Error Reporting Program (CERP), along with a multitude of product error databases at ECRI. By analyzing these comprehensive databases, we help identify and mitigate potential risks with your products and others in the category, ensuring safer products, more receptive end-user clinicians, and more efficient regulatory applications.
Ongoing error research and safety reviews
MSB leverages ECRI and ISMP sources, in addition to external sources like Manufacturer and User Facility Device Experience (MAUDE), to provide tailored error research and safety reviews focused on specific products, product classes, and competitor products. Quarterly, biannual, and annual reports and insights ensure that manufacturers stay informed about emerging safety risks so they can act swiftly to maintain product safety.
Expert guidance to ensure swift implementation of safety improvements, enhancing product effectiveness and boosting clinician receptivity.
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