Page History
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- Complete clean Protocol document
- IRB Approval
- List of Participating Sites (if not included in the protocol document). Multi-site trials require a list of participating sites and contact information.
Informed Consent (if not included in the protocol document)
Currently, the system requires you are required to supply each of your documents as one of the following formats:
- Microsoft Word (.doc, .docx, or .docm),
- Adobe PDF,
- Microsoft Excel (.xls, .xlsx, .xlsm, or .xlsb),
- and/or WordPerfect files.Â
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Adobe PDF files require special processing. For information about creating PDFs, refer to Converting Trial-Related Documents to PDFs. |
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