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Subject: Critical Documents и signed receipt of IB and any current updates hereof pharm. Помогите, пожалуйста, перевести название раздела "Critical Documents" в протоколе клинического исследования и "signed receipt of IB, and any current updates hereof"Critical Documents.
Before the Investigator starts the trial (i.e. the site has green light for screening subjects), the following documents must be available to ХХ:
• regulatory approval and/or notification as required
• curricula vitae of Investigator and Sub-investigator(s) (current, dated and signed and/or supported by an official regulatory document)
• signed receipt of IB, and any current updates hereof ХХ- название компании,
IB -брошюра исследователя
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