E-Consent is a multipurpose, scalable, electronic informed consent system that can be used in a multitude of settings. The platform allows research staff to easily upload multimedia information about a research protocol together with an approved informed consent. These materials are then delivered to potential study participants electronically, in an easy-to-understand and user-friendly way. The system is compatible with a wide range of devices and display sizes, including tablets, mobile devices, laptops, desktops, and others. Further details are available at https://www.ncbi.nlm.nih.gov/pubmed/31349301.
E-Consent has been developed in collaboration with the Mount Sinai IRB to ensure regulatory compliance: IRB-19-02049 Assessment of Multipurpose Scalable Electronic Informed Consent Platform.
If you would like to explore and/or use this offering for your research projects, please open a CRIO / e-Consent ticket at http://osticket.mssm.edu/support/. Irena Parvanova, PhD, or Anar Poltinnikov will respond.
Please be prepared to provide the following documentations to ensure IRB compliance.
- Full IRB-approved protocol
- Letter of approval
Free for all clinical for all clinical research projects
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