Common use of Nežádoucí příhody Clause in Contracts

Nežádoucí příhody. The Investigator shall report adverse events and serious adverse events as directed in the Protocol and by applicable laws and regulations. The Investigator shall cooperate with Sponsor in its efforts to follow-up on any adverse events. The Site shall comply with its LEC reporting obligations. Sponsor will promptly report to the Site, the Site’s LEC, and IQVIA, any finding that could affect the safety of participants or their willingness to continue participation in the Study, influence the conduct of the Study, or alter the Site’s LEC approval to continue the Study.

Appears in 3 contracts

Samples: Trial Agreement, Trial Agreement, Clinical Trial Agreement

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Nežádoucí příhody. The Investigator shall report adverse events and serious adverse events as directed in the Protocol and by applicable laws and regulations. The Investigator shall cooperate with Sponsor in its efforts to follow-up on any adverse events. The Site shall comply with its LEC reporting obligations. Sponsor will promptly report to the Site, the Site’s LEC, and IQVIALEC , any finding that could affect the safety of participants or their willingness to continue participation in the Study, influence the conduct of the Study, or alter the Site’s LEC approval to continue the Study.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Nežádoucí příhody. The Investigator shall report adverse events and serious adverse events as directed in the Protocol and by applicable laws and regulations. The Investigator shall cooperate with Sponsor in its efforts to follow-up on any adverse events. The Site shall comply with its LEC reporting obligations. Sponsor will promptly report to the Site, the Site’s LEC, and IQVIAQuintiles, any finding that could affect the safety of participants or their willingness to continue participation in the Study, influence the conduct of the Study, or alter the Site’s LEC approval to continue the Study.

Appears in 1 contract

Samples: Clinical Trial Agreement Smlouva O Klinickém Hodnocení

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