Regulaido by Pharos Labs

Regulaido is a medical writing and document automation tool developed by Pharos Labs, designed to support life sciences teams working on market access dossiers, systematic literature reviews (SLRs), and regulatory submissions. It combines agentic AI capabilities with built-in evidence tracking and compliance features, enabling medical writing teams to produce higher-quality outputs more efficiently while meeting the standards required in regulated environments.

Agentic AI Chat with Evidence Traceability

• Allows users to upload source documents such as clinical study reports, guidelines, and publications, then query them using natural language.
• AI-generated responses include citations that link directly back to exact passages within the uploaded source documents, reducing the risk of unsupported claims or hallucinations.
• Designed to provide verifiable, traceable answers rather than generative responses disconnected from source material.

Systematic Literature Review (SLR) Workflow

• Supports database searching across PubMed and other literature databases directly within the platform.
• Uses AI to screen thousands of abstracts, significantly reducing the manual effort involved in the screening phase.
• Automatically fetches full-text PDFs for relevant records identified during screening.
• Extracts structured data from full-text sources to support evidence synthesis.
• Maintains human oversight at each stage, with subject matter experts able to review and verify AI-assisted decisions throughout the workflow.
• Aims to compress SLR timelines from months to days.

Compliance and Enterprise Readiness

• ISO 27001 certified, reflecting adherence to internationally recognised information security management standards.
• Supports Azure Active Directory (Azure AD) single sign-on (SSO) for enterprise identity management.
• Provides full audit trails to support documentation and review requirements in regulated settings.
• Includes validation support documentation to assist teams undertaking GxP validation processes.
• Offers data residency control, allowing organisations to manage where their data is stored in line with internal or regulatory requirements.

Regulaido is positioned for life sciences organisations that require both the efficiency gains of AI-assisted workflows and the auditability, security, and compliance infrastructure expected in regulated medical writing and market access contexts.