Increase efficiencies and productivity by automating core reporting tasks for medical writing.
Automate core regulatory report documents across the CTD pyramid and dramatically accelerate submission timelines.
Incredible news: Yseop has been named to Fast Company’s World Changing Ideas list! We’re
honored to be recognized among organizations making a difference in the world.
Yseop named to Fast Company’s 2026 World Changing Ideas list Read More »
Yseop was recently featured in mind Health, where Pierre-Louis Durel, VP Strategy & Operations, shared how AI is transforming regulatory writing—and why it is becoming a critical lever for accelerating access to new therapies.
Yseop Featured in mind Health: Accelerating Drug Approvals with Regulatory-Grade AI Read More »
Yseop wins the 2026 BIG Innovation Award, recognized for transforming regulatory writing with GenAI
The promise of AI in pharma has been circulating for years. In 2025, the industry stopped talking about potential and started designing around it.
2025: The Year Pharma Crossed the AI Threshold Read More »
Yseop recognized by TIME for transforming how life sciences teams create regulatory documents with AI automation.
TIME Names Yseop Copilot One of the Best Inventions of 2025 Read More »
Yseop’s first CMC-focused offering automates the Quality Overall Summary (Module 2.3), a central component of regulatory submissions that pulls structured insights from Module 3.2.
Yseop Expands into CMC: Redefining Regulatory Automation Beyond Clinical Read More »
Listen to the next episode of AI Uncovered with Karla Childers.
Karla Childers – Ethical Guardrails for AI in Pharma Read More »
The FDA has begun using generative AI to review drug submissions, signaling a major shift in regulatory review. Learn how this impacts pharma teams and what it takes to make your content AI-ready.
Listen to the thirteenth episode of AI Uncovered with Emmanuel Walckenaer
Listen to the twelfth episode of AI Uncovered with Emmanuel Walckenaer