Dry Biobank

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Relative registration forms should be filled when clinical data is used. Relative forms include registration form for data entry of Biobank and registration form for data out of Biobank.

 

Documentation Required For the clinical data

Supporting Documentation Requirement

Research dataset

Biospecimens associated clinical data

Summary of research plan (protocol)

Required

IRB review (from applicant’s institution)

Written approval from the requestor’s IRB must be submitted stating that the IRB has either a) performed a review of the project and issues an approval, or b) declared that the research project is exempt from review.

Online request form

Required; Application form for the use of Biobank Database; Registration form for the use of Biobank Database

Signed Informed consent

Required