Consent Creation

DrugDev offers the industry’s first ever SaaS solution for informed consent. SaaS consent gives study teams the tools, training and best practice resources they need to create, manage and automate consent solutions in-house with…

  • Self-managed system allows clients to create new trials, add sites, produce consent documents, manage access controls, reporting, & more
  • Comprehensive management and control of the complete ICF authoring, review and approval process
  • Configurable role-based workflows, including due dates, checklists and audit trails
  • Guided ICF creation using templates, Word documents, prior ICFs, or built from scratch
  • Unlimited trials, add/remove sites, manage access controls, and more
  • Flexible deployment onto any tablet or device at sites, including those already in use (e.g. ePRO/eCOA)
  • Output any consent form to paper
  • A centralized authoring process that eliminates all issues with different form versions
  • Intuitive structured form fields, progression checks, and wizard capabilities
  • Document attributes are carried across global master, country-level, and site-specific ICFs

Marrying the proven benefits of eConsent with an interface as intuitive as Microsoft Word, Consent Creation streamlines the time and cost of development and implementation, enabling sponsors and CROs to bring the proven benefits of eConsent to millions more patients worldwide.