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Source & informed Consent TECHNOLOGY UTILIZATION AT TRIAL SITESClinical Systems Technology Marketplace 2015 Peggy SiemonHryczyk, PhD, Overview for Site of Tablet and Portal CRF Fields Web Portal
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Esource amp einformed consent is a digital platform for obtaining study participants’ informed consent electronically.
Research institutions and organizations conducting clinical trials are required to file esource amp einformed consent.
Esource amp einformed consent can be filled out online by the participants with the help of a research coordinator or investigator.
The purpose of esource amp einformed consent is to ensure that study participants are fully informed about the study, its risks, benefits, and their rights before agreeing to participate.
Esource amp einformed consent must include information about the study objectives, procedures, risks, benefits, confidentiality, and participant rights.
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