NoxReg's mission is to make pharmaceutical regulatory intelligence accessible to every pharma, biotech, and CRO team — regardless of size or budget. We believe no team should miss a critical regulatory update because they lacked the tools to monitor it.
Our story
NoxReg was founded in 2025 after watching regulatory affairs teams manually refresh 30+ agency websites every morning, copy-pasting updates into shared spreadsheets, and still managing to miss critical safety notices published out of hours. The problem was not a lack of effort — it was a lack of infrastructure.
We built NoxReg to solve this — an always-on intelligence layer that monitors every major health authority automatically, classifies updates by importance, and delivers what matters directly to your team. What took two hours a day now takes ten minutes. What was missed is now flagged before anyone opens a browser.
Every feature in NoxReg is designed with one question in mind: will this help a regulatory professional make a better decision, faster? If the answer is yes, we build it. If it adds noise without clarity, we do not.
The team
CEO & Founder
Regulatory intelligence expert. Built NoxReg to give every pharma team the monitoring capability previously only available to the largest organisations.
LinkedIncontact@noxreg.comOur values
We'd rather deliver one correct alert than ten uncertain ones. Regulatory decisions have real consequences — we take that responsibility seriously.
AI assists, humans decide. Every output is a starting point, not a conclusion. We build tools that augment regulatory professionals, never replace their judgment.
Every design decision accounts for GxP, GDPR, and audit requirements. We understand that our customers operate in environments where compliance is not optional.
Join regulatory teams across Europe and North America who use NoxReg to stay ahead of every health authority update.