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Comment: For CTRPMICRO-368, revised based on JIRA description.

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titleValidate the regulatory information for Complete trials that require XML documents for submission to ClinicalTrials.gov.

These instructions pertain to Complete trials. Regulatory information validation does not pertain to Abbreviated

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These instructions pertain to complete trials that require XML documents for submission to ClinicalTrials.gov.

How to Validate Regulatory Information

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