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Ritivel

Ritivel is a YC Winter 2026 (W26) company. Based in San Francisco, CA, USA. Team of 3.

  • Generative AI
  • Compliance
  • Enterprise Software
  • Regtech
  • Biotechnology

About Ritivel

GPAgent's own fund-neutral profile, written from public information. Updated Oct 4, 2026.

Summary

Ritivel builds AI agents that draft regulatory submission documents for life sciences companies, producing first drafts of filings such as CTDs, CSRs, INDs, and BLAs directly in Microsoft Word. The agents pull clinical data and prior submissions from connected systems like SharePoint and Veeva, embed citations traceable to source documents, and handle follow-up communications through Outlook. The product replaces a manual, months-long process in which regulatory and medical writing teams must gather scattered documents, consolidate clinical data, and compose dense submissions by hand.

Go-to-market

Regulatory and medical writing teams at pharmaceutical and life sciences companies are the primary buyers, reached through direct outreach informed by extensive interviews with pharma professionals.

From the Y Combinator listing

How Ritivel describes itself in Y Combinator's public directory.

AI-native platform for Life-Sciences Documentation

Ritivel is an AI-native workspace for regulatory and medical writing teams at life sciences companies. Our AI agents draft CTDs, CSRs, INDs, and BLAs in minutes instead of weeks, helping drugs reach patients faster. Every month a drug is delayed from reaching the market costs pharma companies ~$45M in lost revenue and more importantly, delays treatment for thousands of patients who need it. Yet regulatory teams are stuck in a painful, months-long process: synthesizing thousands of pages of clinical data, hunting through SharePoint folders for the right documents, chasing colleagues for missing inputs, and manually drafting submissions. Ritivel deploys AI agents that transform how regulatory teams work. Our agents generate comprehensive first drafts directly in Microsoft Word, following FDA formatting requirements and pulling from your existing clinical data and prior submissions. Every data point includes citations linked back to the original source, so reviewers can verify with one click. Connected to SharePoint and Veeva, our agents automatically source the right documents. Integrated with Outlook, they handle reminder emails and follow-ups automatically. We're engineers who previously built AI copilots at Microsoft Research. After 50+ conversations with pharma professionals, we discovered the critical bottleneck in regulatory submissions and built Ritivel to solve it.

Facts

Industry
Healthcare / Healthcare -> Healthcare IT
Location
San Francisco, CA, USA
Team size
3
Status
Active
Stage
Early

Founders (3)

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