Almac's Trial Coordinator: eConsent Platform For Modern Clinical Trials

Informed consent is often slowed by paperwork, site visits, and manual tracking—creating delays in enrollment and added administrative burden for research teams. Ensuring participants, including minors, vulnerable adults, and legal representatives, truly understand what they're agreeing to while meeting strict regulatory requirements adds further complexity to an already demanding process.

eConsent addresses this by digitizing the consent journey, combining secure electronic signatures, full audit trails, and real-time status tracking with an intuitive experience for participants of all ages. Built-in support for remote and in-person consent, flexible re-consent workflows, and compliance with 21 CFR Part 11 and GDPR help sites accelerate enrollment while maintaining data integrity. For teams looking to reduce delays and improve participant understanding throughout the consent process, a protocol-adaptive eConsent approach offers a clear path forward. Explore how digitizing consent can simplify compliance and keep studies moving.