Features
AI-accelerated FDA submission authoring
Regulatory pathway strategy & roadmap
End-to-end submission support (510(k), De Novo, PMA, IND, NDA, BLA)
Pre-FDA meeting preparation and participation
FDA-trained AI for document analysis and drafting
100% expert oversight by ex-FDA consultants
Fixed, milestone-based pricing
Combines human expertise with custom AI tools
Supports medical devices and pharmaceuticals
Timeline compression (claims 60% faster than incumbents)
Dedicated regulatory lead assigned per project
Free initial consultation to scope work
Journal via text, voice, or photo import
Emotional analysis using Plutchik's framework
Personality insights based on Big Five model
Recurring topic detection and trend overview
Chat with your journal history (Ask Your Journal)
AI-generated artworks from journal entries
50+ mental model templates (First Principles, Ikigai, etc.)
Voice mode for hands-free journaling
Smart Editor with personalized prompts and comments
Weekly review email summaries
Minds: virtual personas providing feedback
Habit tracking and automatic summaries
Encrypted at rest and in transit
Available on web, iPhone, Android
