eConsent: Start Planning Now for the Inevitable

Whitepaper | eConsent: Start Planning Now for the InevitableThe research community is on the brink of a revolution. Today, the process of enrolling trial participants and documenting informed consent involves long paper documents, multiple wet signatures, frequent revisions, and long-term paper archives. It’s time for researchers and sites to begin planning for the inevitable shift to a paperless informed consent process.

This whitepaper discusses the definition and value of eConsent, the regulatory requirements around eConsent, and review and approval of eConsent by the IRB.

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