eConsent is an electronic informed consent system (eConsent) designed by Landmark Research, which is offered as a software as a service (SaaS) for its clients to perform eConsenting of subjects and manage their site visits for clients in their clinical studies.

eConsent is a web-based platform that allows the users to perform the following functions:

• eConsenting
  & Compliance

  eConsent enables users to obtain and document informed consent using interactive multimedia forms, customizable according to study protocols. It ensures compliance with ethical and regulatory standards including Declaration of Helsinki, ICH GCP, and HIPAA.

• Site Visit
  Management

  eConsent enables users to schedule and manage site visits using calendars, reminders, notifications, and checklists. It allows monitoring and tracking of visit progress, status, outcomes, and results for efficient site visit management.

• Multi-device
  & Language Support

  eConsent supports various languages, formats, and devices including tablets, smartphones, and computers, ensuring accessibility and user satisfaction across different platforms and demographics.

Talk to our eConsent experts

Speak with our eConsent specialists to learn more about our electronic informed consent system, request a demo, or get help with implementation. Our dedicated team is ready to assist you with all your clinical trial consent management and site visit coordination needs.

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