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submittrialdoc
submittrialdoc
When registering Complete trials, you must upload the following types of documents:

  • 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.

Note
titleSpecial processing for PDF files

Adobe PDF files require special processing. See the information about creating PDFs in Converting Trial-Related Documents to PDFs.

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