Panacea
AI-Native FDA Regulatory Services
About Panacea
Panacea provides AI-native FDA regulatory services for Biotechs and Medical Device companies. We hire the most experienced FDA consultants in the industry (ex-FDA, decades of experience, hundreds of filings) and pair them with our AI platform to enable the fastest and lowest cost pathway to FDA approval. While other regulatory consultants bill hourly, our pricing model is simple: fixed, outcome-based pricing. Payment is only due when milestones are complete. We support all FDA regulatory pathways including IND, NDA, BLA, ODD, Pre-Subs, 510(k), De Novo, PMA, IDE, BDD, etc.
Public traction evidence
Each signal links to the public source used for attribution.
- X
Aaron Epstein X post about Panacea
FDA approval can take years and costs millions. Most of that is slow, manual regulatory work billed by the hour. @withpanacea gives the best FDA consultants AI superpowers, and cuts timelines in half. Every day faster = more patients helped sooner.
- LinkedIn
Two million people die every year from cancers that an early diagnosis could have prevented.
[Skip to main content](https://linkedin.com/posts/panacea-bio_two-million-people-die-every-year-from-cancers-activity-7482811206714699776-QNaz#main-content)[LinkedIn](https://linkedin.com/?trk=[redacted-public-param]) * [Top...
- YouTube
Panacea Launch Video
Introducing Panacea: AI-Native FDA Regulatory Services for faster, lower cost FDA filings and approval. https://withpanacea.com/