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submittrialregulatory
submittrialregulatory
Complete this section only if you require an XML document to register your trial with ClinicalTrials.gov.
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How to Complete the Regulatory Information Section

Select or enter the appropriate information in the text fields and drop-down lists. The following table describes the fields. An asterisk (*) indicates a required field. For a definition of each field. See the ClinicalTrials.gov Protocol Data Element Definitions for definitions for these fields, refer to http://prsinfo.clinicaltrials.gov/definitions.html.

Instructions for recording regulatory information

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