TrialForge streamlines protocol development from study design to regulatory submission. Collaborate with your team, ensure compliance, and export publication-ready documents — all in one platform.
Build study designs with support for parallel, crossover, adaptive, and more trial types. Manage arms, endpoints, and criteria visually.
Review workflows, threaded comments per section, version tracking, and role-based access keep your team aligned throughout.
Built-in checklists for ICH-GCP, FDA 21 CFR, and EMA guidelines help you stay audit-ready from day one.
Generate publication-ready PDF and Word documents with customizable section selection and professional formatting.