We’ve reimagined how clinical trial documents get built and generated. Not just faster, better, and fully adapted to your processes. Make documentation work with your processes and workflows, not the other way around. Custom templates are how you encode that decision once, and execute it consistently across every protocol.
Custom Content Templates
Clinials custom templates are structured, compliance-aligned content blueprints that allow organisations to standardise how protocol-derived information is transformed into outward-facing materials, without losing governance, brand control, or regulatory alignment. Build them yourself or let us help you!
How it works
Empower your teams with tailored reports and documents that enhance clarity, improve collaboration, and support faster decision-making across every stage of your trial.
Tell us what’s not working
What do you need this document to do that it doesn’t do today?
We help you configure it
We’ll collaborate on structure, content types, layout, and logic.
You get a working version
Inside your account. Version-controlled. Ready to use. Ready to share.
What you can build
Here’s what early users are already creating:
Finance-friendly feasibility sheets
Compliance-specific content packs
Risk planning summaries
Plain language summaries with marketing polish
Patient sheets aligned with real-world templates
Create Organizational Templates
Instead of generating generic outputs, custom templates: Define the exact structure of the document (sections, ordering, required fields) Embed organisation-specific language, tone, and positioning Lock in compliance statements and mandatory disclaimers Align to internal SOPs, brand guidelines, and regulatory frameworks Control how extracted protocol data is translated into plain language