Reporting of SAEs by the investigational sites to the Company or the Charity, as the case may be Sample Clauses

Reporting of SAEs by the investigational sites to the Company or the Charity, as the case may be. The Company shall, if it (or any of its licensees or sub-licensees) is carrying out clinical trials on Related Products, use all reasonable endeavours to · monitor, and ensure that it receives from the investigational site within twenty four (24) hours of the investigator or any member of the study team becoming aware of the event) initial reports on SAEs from clinical trials of the Related Products; and · actively seek follow-up information from the investigational site on SAEs from clinical trials of the Related Products until full details (including diagnosis if available, causality, outcome and cause of death if fatal) are reported. The Charity shall use all reasonable endeavours to: · monitor, and ensure that it receives from the investigational site within twenty four (24) hours of the Principal Investigator or any member of the study team becoming aware of the event) reports on SAEs from the Clinical Trial; and · actively seek follow-up up information from the investigational site on SAEs from the Clinical Trial until full details (including diagnosis if available, causality, outcome, and cause of death if fatal) are reported.
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Related to Reporting of SAEs by the investigational sites to the Company or the Charity, as the case may be

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