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Recording Trial-Related Documents

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MultiExcerptNamesubmittrialdoc

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

  1. Complete clean Protocol document
  2. IRB Approval
  3. List of Participating Sites (if not included in the protocol document). Multi-site trials require a list of participating sites and contact information.

  4. 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 Documents to PDFs .

Trial Related Documents section of the Register Trial pageImage Removed

How to Submit Trial Related Documents

Include Page
CTRP:Uploading Trial-Related Documents - Include v4.4
CTRP:Uploading Trial-Related Documents - Include v4.4

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Navigate to, and select, the appropriate document, and then click Open.

Info

Depending on your operating system, you may see a different command name for "Open."

Repeat the steps above for each type of document.

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titleAdding Multiple "Other" Documents

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Converting Documents to PDFs

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