Consent for specimen collection and data banking. Covers future research use, genetic information provisions, and long-term storage with withdrawal options.
The Biobank/Data Repository consent template addresses the complex considerations involved in collecting and storing biological samples and health data for future research. It provides comprehensive coverage of specimen handling, genetic testing implications, and participants' ongoing rights.
With ten detailed sections, this template covers introduction, biobank purpose, what will be collected, sample usage, genetic information provisions, risks, benefits and compensation, privacy protections, withdrawal procedures, and contact information. Special attention is given to explaining how samples may be used for studies not yet planned.
The genetic information section is particularly important, explaining GINA protections against discrimination, whether results will be returned to participants, and how genetic data will be safeguarded. This transparency is essential for building participant trust in biobanking initiatives.
This template is suitable for academic biorepositories, hospital-based biobanks, disease-specific specimen collections, and multi-institutional data sharing initiatives.
This is a preview of the complete consent form experience participants will see.
Please provide your contact details
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Signature Area
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This template addresses the unique consideration that biobank samples may be used for research that hasn't been planned yet.