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Semantic Infrastructure 2.0 needs to address metadata and terminology related requirements from the life sciences domain. This will enable interoperability both between different sub-domains within life sciences, and between life sciences and other domains in caBIG® such as clinical trials and electronic health records. While life sciences will leverage common semantic functionalities such as Enterprise Conformance and Compliance Framework (ECCF) registry, modeling, forms, behavioral semantics, terminology and value sets, there are aspects specific to the life sciences domain that need to be addressed, including but not limited to:

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• Participating consortium sites each submit common consent forms, case report forms, and boilerplate Material Transfer Agreements (MTA) to the appropriate local regulatory offices.

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• Patients are followed for 3 three years from primary treatment date. An annual follow-up visit occurs and a blood sample is taken. Additional clinical annotations are collected.

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