DEFINITIONS. 1.1 “Adverse Event” shall mean any unfavourable and unintended sign (including, for example, an abnormal laboratory finding), symptom, or disease temporally associated with the use of a Product, whether or not considered related to the Product, it shall also include any clinically significant worsening of a pre-existing condition and any lack or loss of intended effect.
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Samples: Sales Contracts, Sales Contracts, Sales Contracts