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CDMRAFORMCDM registry holding account opening request form (Version 02.0) This form is to be used by project participants authorized by an Annex I Party to request the opening of a permanent holding
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CDM stands for Clinical Data Management, and a CDM registry is a system used for collecting, managing, and analyzing clinical trial data to ensure its integrity and compliance with regulatory standards.
All clinical trial sponsors and investigators who are conducting studies that involve human subjects are required to file with the CDM registry, ensuring that their studies are registered and data is reported.
To fill out the CDM registry, follow the online submission guidelines provided by the registry, ensuring to include all required fields such as trial identifier, sponsor information, and study details.
The purpose of the CDM registry is to promote transparency in clinical research, enhance data integrity, and allow for easy access to crucial information about ongoing and completed clinical trials.
Required information includes trial title, description, recruitment status, study design, eligibility criteria, and contact information for the study team.
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