Any unintentional error in the prescribing, dispensing, or administration of a medicinal product while under the control of a healthcare professional, patient or consumer (EMA-PRAC Good Practice Guide on Recording, Coding, Reporting and Assessment of Medication Errors, 23 October 2015).
Other glossary definitions
B
Biometric data
Under the GDPR, biometric data is considered to be sensitive data and to that extent…
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M
MA (Marketing Authorisation)
Marketing authorisation is the process of reviewing and assessing the evidence to support a medicinal product,…
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