№ lp_1_2_52799
This document outlines the procedures for designing Case Report Forms (CRFs) in clinical trials, including both paper and electronic versions, with a focus on ensuring accurate data capture and analysis.
Year: 2019
Region / city: Not specified
Subject: Clinical trial documentation, Case Report Form (CRF) design
Document type: SOP (Standard Operating Procedure)
Organization: ALERRT (Association for Data Management in the Tropics)
Author: Hanne Landuyt
Target audience: Clinical trial staff, Data managers, Investigators
Period of validity: Not specified
Approval date: 01/02/2019
Revision date: 10/10/2019
Date of changes: 20/06/2022
Price: 8 / 10 USD
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