Common use of Reporting Adverse Events and ICH GCP Breaches Clause in Contracts

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 8.

Reporting Adverse Events and ICH GCP Breaches. Institution Provider and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 10.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report ICH GCP breaches as well as adverse events experienced by Trial Study Subjects at any time in accordance with instructions in the Protocol and Applicable Law.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 7. Hlášení nežádoucích příhod a porušení ICH GCP Zdravotnické zařízení a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 10.

Reporting Adverse Events and ICH GCP Breaches. Institution will immediately and Principal Investigator will report fullyreport adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 8.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 9. Hlášení nežádoucích příhod a porušení ICH GCP Zdravotnické zařízení a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. Hlášení Nežádoucích Příhod a Porušení ICH GCP. Zdravotnické zařízení a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will promptly report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.

Reporting Adverse Events and ICH GCP Breaches. Institution Provider and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 9. Hlásenie nežiaducich udalostí a porušení usmernení Medzinárodnej konferencie o harmonizácii pre správnu klinickú prax. Inštitúcia a zodpovedný skúšajúci budú vždy hlásiť nežiaduce udalosti, ktoré sa prejavia u účastníkov skúšania, v súlade s pokynmi uvedenými v protokole a platnej legislatíve.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions Applicable Law. in the Protocol and Applicable Law.and

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report ICH GCP breaches as well as adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.

Reporting Adverse Events and ICH GCP Breaches. Institution Provider and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 7. Hlášení nežádoucích příhod a porušení ICH GCP Poskytovatel a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.7. Hlášení nežádoucích příhod a porušení ICH GCP Zdravotnické zařízení a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable LawLaws and Regulations.

Reporting Adverse Events and ICH GCP Breaches. Institution and Principal Investigator will report adverse 7. Hlášení nežádoucích příhod a porušení ICH GCP. Poskytovatel a hlavní zkoušející nahlásí kdykoliv events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution Provider and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law. 9. Hlášení nežádoucích příhod a porušení ICH GCP. Poskytovatel a hlavní zkoušející nahlásí kdykoliv nežádoucí příhody subjektů klinického hodnocení v souladu s pokyny protokolu a platnými zákony.

Reporting Adverse Events and ICH GCP Breaches. Institution Provider and Principal Investigator will report adverse events experienced by Trial Subjects at any time in accordance with instructions in the Protocol and Applicable Law.and