Sub-Investigator Clause Samples
The Sub-Investigator clause defines the role and responsibilities of individuals who assist the principal investigator in conducting a clinical trial or research study. It typically outlines the qualifications required for sub-investigators, the scope of their permitted activities, and the process for their appointment or removal, such as requiring sponsor approval or notification. This clause ensures that all personnel involved in the study are properly authorized and qualified, thereby maintaining the integrity of the research and compliance with regulatory requirements.
Sub-Investigator any individual member of the Study team designated and supervised by the Investigator at a Study site to perform critical trial- related procedures and/or to make important Study-related decisions.
Sub-Investigator any individual member of the Study team designated and supervised by the Investigator at a Study site to perform critical trial- related procedures and/or to make important Study-related decisions. 5. Hodnocené léčivo - Léčivá ▇▇▇▇▇ upravená do lékové formy nebo placebo, jež jsou testovány nebo použity jako kontrola v Klinické studii, včetně registrovaného léčivého přípravku, pokud ▇▇ ▇▇▇▇▇ používán nebo připraven způsobem odlišným od schválené lékové formy (v jiné lékové formě či balení), ▇▇▇▇ ▇▇-li užit v neschválené indikaci či za účelem shromažďování dalších informací o schváleném použití.
Sub-Investigator any individual member of the Study team designated and supervised by the Studie. Informovaný ▇▇▇▇▇▇▇ ▇▇ dokumentován formou písemného, podepsaného a datovaného formuláře.