OHLAŠOVACÍ POVINNOST. Institution and Investigator shall strictly comply with the adverse event provisions of the Protocol and any applicable local requirements. Any serious adverse events must be reported to Sponsor within 24 hours after first of either Institution and/or Investigator becomes aware hereof.
Appears in 6 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
OHLAŠOVACÍ POVINNOST. Institution and Investigator shall strictly comply with the adverse event provisions of the Protocol and and any applicable local requirements. Any serious adverse events must be reported to Sponsor within 24 hours after first of either Institution and/or Investigator becomes aware hereof.
Appears in 1 contract
Samples: Clinical Trial Agreement