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Annex 2 to the Guidelines Participant personal data form to be entered into the Agency\'s ICT system for the purpose of monitoring project participantsPARTICIPANT PERSONAL DATA FORM to be entered
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Individuals and organizations involved in clinical trials and research
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IT professionals working with computerised systems and electronic data in clinical settings
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What is draft-guideline-computerised-systems-electronic-data-clinical?
draft-guideline-computerised-systems-electronic-data-clinical provides guidance on the use of computerized systems for electronic data in clinical settings.
Who is required to file draft-guideline-computerised-systems-electronic-data-clinical?
Healthcare organizations and clinical research facilities are required to file draft-guideline-computerised-systems-electronic-data-clinical.
How to fill out draft-guideline-computerised-systems-electronic-data-clinical?
Draft-guideline-computerised-systems-electronic-data-clinical can be filled out online through the designated government portal.
What is the purpose of draft-guideline-computerised-systems-electronic-data-clinical?
The purpose of draft-guideline-computerised-systems-electronic-data-clinical is to ensure the proper use and management of electronic data in clinical settings.
What information must be reported on draft-guideline-computerised-systems-electronic-data-clinical?
Information such as the type of computerized system used, data security measures, and data validation methods must be reported on draft-guideline-computerised-systems-electronic-data-clinical.
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