Accelerator
Tryal Accelerator helps CROs and biopharma companies accelerate the creation of key study documents, transforming content generation to cut costs, save time and reduce risk. By replacing manual drafting, companies can improve document consistency, streamline mid-study changes, and accelerate the path from study startup to conduct.
AI-enabled document generation, contextual assistance, and workflow integration for clinical development teams.
Common Documents Accelerated
Accelerator is built to generate the complex documents required for study startup and speed up time to finalization.
Informed Consent Form (ICF)
Data and safety monitoring plan (DSMP)
Data Management Plan
Recruitment Plan
Training recruiting materials
Risk Management Plan
Clinical monitoring plan
Site Contract and Budget Plan
Protocol Deviation plan
Safety monitoring/management plan
Statistical Analysis Plan
Site Training Materials
Project Management Plan and Comms Plan
Site Identification Plan and Site Feasibility Plan
Draft CRF’s
- Edit check specs
- CRF Completion guidelines
- CRF design specs
Investigator Brochure
TMF Plan
Subject Information Sheet
Data Privacy Plan
Quality Plan
Monitoring visit report template
Device User Manual
IP Instructions for Handling
IP Supply Plan
IP Directions for Use
IP Instructions for Handling
IP Manual
Pharmacy Manual
Device Packing Insert Instruction For Use
IP Recall Documentation
IP Recall Plan
Non-IP Supply Plan
Laboratory plan
Medical Monitoring Plan
Data surveillance Plan
Regulatory Project Plan (translation, submission requirements, timing, etc.)
Strategic Data Review Plan
Unblinding plan
Vendor Management Plan
RFP Generation
Comprehensive Document Generation from Curated Inputs
Tryal’s agentic model drives the initial generation of each document, applying the right logic, context, and validation rules based on study configuration. From there, users can edit and revise content within an integrated workflow, with AI support available throughout. The result is high-quality, study-aligned output without added complexity.
Study-Specific Knowledge Base with Controlled Scope
Tryal uses a dedicated, study-specific knowledge base built only from sponsor-provided materials like documents, transcripts, and emails. This ensures outputs are grounded in approved content and avoids hallucinations. When configured, generation is limited to this curated input for precise, controlled, and traceable results.
Impact Analysis Across Documentation
When something changes, such as a visit, a procedure, an instrument, Tryal can assess and surface all related documents that may be affected. This in-progress feature gives teams a scalable way to maintain alignment, reduce rework, and avoid downstream inconsistencies as trials evolve.
Compliance
and Traceability
By Design
Inputs, actions, and outputs in Tryal are structured and traceable by default. This enables alignment with 21 CFR Part 11, supports GxP documentation expectations, and provides audit-ready transparency, even when AI is involved.
