Waiver of Consent. In the event that Company has requested a waiver of the consent and/or authorization requirement, as set forth in applicable law, from each clinical site’s IRB, no clinical trial may be conducted by Company pursuant thereto until each clinical site’s IRB has issued appropriate documentation of such waiver in accordance with applicable law. Company shall maintain a true copy of the documentation of such waiver to be made available within ten (10) days upon written request by LLS.
Appears in 3 contracts
Samples: Definitive Agreement, Definitive Agreement (Celator Pharmaceuticals Inc), Definitive Agreement (Celator Pharmaceuticals Inc)
Waiver of Consent. In the event that Company has requested a waiver of the consent and/or authorization requirement, as set forth in applicable law, from each clinical site’s IRB, no clinical trial may be conducted by Company pursuant thereto until each clinical site’s IRB has issued appropriate documentation of such waiver in accordance with applicable law. Company shall maintain a true copy of the documentation of such waiver to be made available within ten (10) ** days upon written request by LLS.
Appears in 2 contracts
Samples: Definitive Agreement (Onconova Therapeutics, Inc.), Definitive Agreement (Onconova Therapeutics, Inc.)
Waiver of Consent. In the event that Company has requested a waiver of the consent and/or authorization requirement, as set forth in applicable law, from each clinical site’s IRB, no clinical trial may be conducted by Company pursuant thereto until each clinical site’s IRB has issued appropriate documentation of such waiver in accordance with applicable law. Company shall maintain a true copy of the documentation of such waiver to be made available within ten (10) [**] days upon written request by LLS.
Appears in 1 contract
Samples: Definitive Agreement (Curis Inc)