LogicFlo AI offers modular AI agents that automate research, writing, and review tasks for medical‑affairs content, ingesting data from PubMed, Veeva, and SharePoint to generate slide decks, manuscripts, and CME materials with auditable citations. The platform includes built‑in compliance checks aligned with SOPs and regulatory standards (SOC 2, ISO 27001, HIPAA) and a human‑in‑the‑loop review step, delivering drafts up to 2,000× faster while maintaining traceability.
Funding
$2.7M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Life sciences professionals spend extensive time on manual content creation—formatting documents, validating references, and managing version control—while strict regulatory compliance demands auditable citations and traceability. This bottleneck slows the delivery of MSL decks, training materials, journal drafts, and other medical‑affairs deliverables.
Solution
LogicFlo AI provides a fleet of task‑specialized AI agents that act as virtual teammates for medical‑affairs workflows. Each “desk” (Research, Writing, Review) autonomously ingests data from sources such as PubMed, Veeva, and SharePoint, generates scientifically accurate slide decks, manuscripts, and CME content, and embeds fully auditable citation metadata. The platform enforces compliance by applying built‑in SOP checks, SOC 2/ISO 27001/HIPAA‑aligned security controls, and a human‑in‑the‑loop review step before final approval. Integrated APIs enable seamless export to enterprise systems and downstream analytics dashboards, delivering drafts up to 2,000× faster while preserving traceability and regulatory readiness.
Target Audience
Primary users are medical‑affairs teams, Medical Science Liaisons, and medical communications groups within biopharma companies and contract research organizations that require rapid, compliant content production at scale.
Features
- Modular AI “desks” (Research, Writing, Review) that operate as coordinated agents rather than a single assistant
- Direct integration with Veeva, SharePoint, Microsoft Word, and PubMed for data ingestion and document publishing
- Automated generation of slide decks, training modules, congress posters, CME modules, journal drafts, and MLR‑ready content with real‑time citation tagging and reference linking
- Built‑in compliance engine that validates content against SOPs, regulatory checklists, and audit‑trail requirements (SOC 2, ISO 27001, HIPAA)
- Human‑in‑control workflow that surfaces AI suggestions for expert review, ensuring final sign‑off remains with the user
- Customizable output that adapts messaging, data selection, and visual style to specific therapeutic areas, specialties, or HCP preferences
- Cloud‑hosted, end‑to‑end encrypted architecture with role‑based access controls and versioned audit logs for full traceability