AI Companion Tools — IDDCR Global Research
AI-Powered Productivity for CRO Professionals
A suite of intelligent tools purpose-built for clinical research — from document drafting and protocol summarisation to regulatory writing and personalised learning. Available now for CRO teams worldwide.
Intelligent Tools for Every Stage of Clinical Research
AI Companion Tools brings together ten specialist AI modules designed around the real workflows of CRO professionals. Whether you are drafting a clinical study report, mapping CDISC standards, or reviewing pharmacovigilance narratives, each tool is trained on domain-specific knowledge to deliver accurate, audit-ready outputs — faster.
Ten Specialist AI Modules
Each module is purpose-built for a distinct CRO discipline — trained on domain knowledge, aligned to regulatory standards, and ready to use today.
Research Assistant
Accelerate literature reviews, hypothesis generation, and evidence synthesis with an AI assistant trained on clinical and scientific databases. Surface relevant studies, summarise findings, and identify research gaps in minutes.
Scientific Writing
Draft, edit, and refine scientific manuscripts, abstracts, and publications with AI that understands clinical terminology, journal style guides, and regulatory writing conventions.
Clinical Trials Assistant
Summarise protocols, generate informed consent language, draft site initiation visit agendas, and produce study-level summaries — keeping trial teams aligned and audit-ready at every phase.
Data Management
Automate data query generation, annotate CRFs, and produce data management plan sections with AI that understands EDC structures, data standards, and ICH E6(R3) requirements.
Biostatistics Support
Generate statistical analysis plan sections, interpret outputs, and draft results narratives. AI assistance for sample size justification, endpoint definitions, and statistical methodology documentation.
CDISC Standards
Map raw data to SDTM and ADaM domains, generate define.xml annotations, and validate submission datasets against CDISC implementation guides — with AI-guided mapping suggestions.
Pharmacovigilance
Draft SAE narratives, generate CIOMS and MedWatch forms, and support signal detection documentation. AI tools trained on ICH E2A/E2B guidelines and global pharmacovigilance requirements.
Regulatory Compliance
Produce regulatory submission sections, gap analyses, and compliance checklists aligned to FDA, EMA, and ICH guidelines. AI-assisted authoring for CTD modules and regulatory correspondence.
Document Analysis
Upload clinical documents — protocols, CSRs, investigator brochures — and extract key information, flag inconsistencies, and generate structured summaries using AI-powered document intelligence.
Personalised Learning
Adaptive learning pathways for clinical research professionals — covering GCP, CDISC, biostatistics, and regulatory affairs. AI-curated content aligned to your role, experience level, and learning goals.
Why AI Companion Tools?
Domain-Trained Intelligence
Each module is trained on clinical research-specific knowledge — not generic AI. Outputs align with ICH, FDA, EMA, and CDISC standards from day one.
Audit-Ready Outputs
Every document, narrative, and mapping produced is structured for regulatory review — with traceable reasoning and compliant formatting built in.
Seamlessly Integrated
AI Companion Tools works alongside your existing EDC, CTMS, and document management systems — no rip-and-replace required.
Available Now
Fully operational and ready to deploy across your CRO or sponsor team. Contact us to discuss access, onboarding, and tailored configurations.
Ready to Transform Your Clinical Research Workflows?
Speak with our team to explore how AI Companion Tools can be configured for your organisation's specific therapeutic areas, submission timelines, and compliance requirements.