Have a look at this inforgraphic that gives insights on how in the world of clinical trials, effective management of Serious Adverse Events (SAEs) is essential to ensure participant safety and the reliability of study outcomes. A streamlined process encompasses steps from accurate reporting by the investigator to thorough review and approval by relevant authorities, and Asphalion can help you along the process.
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As a company committed to sustainability, we follow the UN’s 2030 Agenda and its Sustainable Development Goals.
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