Empower your team with intelligent drafting, real-time
insights, and a seamless collaboration—all in one platform.
Our AI-powered tools extract relevant data from your own documents in seconds and help you with a first draft of new documents (synopsis, protocols,…)
Reduce redundancy, boost consistency, and save hours of manual effort.
Reduce redundancy, boost consistency,
and save hours of manual effort.
Our tools ensure compliance with global standards and suggest improvements.
Facilitate alignment across teams with structured authoring tools.
Ensure content consistency, streamline approvals, and accelerate timelines.
Grant, revoke, and change access to documents to working groups easily.
Align your teams with our first draft, eliminate endless back-and-forth communication.
Gain visibility into workflows and remove bottlenecks.
Get an easy overview of contributors’ access rights, overall progress etc.
Beat deadlines in the clinical process.
We speed up your work with the help of our writing assistant.
You focus on critical tasks, our AI handles repetitive work.
We increase the quality of your documents by flagging potential mistakes and inconsistencies.
We help you structure your documents with industry regulatory-compliant templates.
Ensure compliance and accuracy without delays.
Documents, internal templates, or existing protocols.
Meeting notes, presentations, video captions.
Our AI assistant provides a first draft based on your inputs.
Existing documents are analysed and enhanced as you write.
Collaborate with your team, get approvals, navigate through the different stages and export submission-ready documents.
Join the future of regulatory writing and streamline your process with AI
TrialCraft BV – Belgium – Registered under number BE1010.925.090
Email: info@trialcraft.health