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 you are required to supply your documents as Microsoft Word (.doc, .docx, or .docm), Adobe PDF, Microsoft Excel (.xls, .xlsx, .xlsm, or .xlsb), and/or WordPerfect files.
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Adobe PDF files require special processing. See the information about creating PDFs in Converting Trial-Related Documents to PDFs. |
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