WitrynaAn adverse event (AE) is any untoward medical occurrence in a patient or clinical investigation subject administered a pharmaceutical product and which does not necessarily have a causal relationship with this treatment.An adverse event can therefore be any unfavourable and unintended sign (including an abnormal laboratory … WitrynaIMCA- DignityDownload-5353 (IMCA DP Event Reporting Form) - Free download as PDF File (.pdf), Text File (.txt) or read online for free. ... of an auxiliary system causes …
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IMCA-Download-15058 (IMCA Publications Catalogue) PDF
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