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Table of Contents

In participant-centric studies, participant data like name, age, sex, etc., is collected along with the specimens. The study can be -

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Expand
titleClick here to view the steps...
  1. Select 'Collection Protocols' from the left side menu or home screen
  2. Click the 'Create' button from the protocol's list page.

  3. Enter the required information according to your study and click the 'Create' button
    Example: Creating a CP for the 'Lung cancer research study.'


Details for all the fields on the CP overview page,

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Sites

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Cardiovascular diseases and risk factors knowledge and awareness in people with type 2 diabetes mellitus: a global evaluation

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Short Title

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Code

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Principal Investigator

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specialized a researcher who supports the management and coordination of clinical research studies. There can be multiple coordinators selected.

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Link to the SOP document uploaded on the university web portal

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Note
titleNote:
  1. The CP level PI and Coordinators will not be assigned roles automatically or by default.
  2. After creating the CP, the admin has to manually assign specific roles to all the users who need to access the CP.

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