By Regulation
For Regulatory Affairs
Connect authority updates with the products they affect
Turn requirements into a product-specific action plan
Compare approved text and artwork; plan for ePI
Plan renewals, variations and PSUR work
For Business Development
Research authorisations, holders and market presence
Compare portfolio coverage and potential new markets
Research protection periods and potential entry dates
The Platform
Research requirements, analyse documents and draft plans
Preview regulatory updates by product and market
Preview portfolio timelines, obligations and fees
Authority fees, calculated per procedure, market & product
Screen candidate medicine names against registers, marks, INN stems and languages
Compare packaging artwork with approved text
All 30 EU and EEA markets and EMA are covered. Tell us where else you file. It takes two minutes.
Pick the regions. Open one to choose single countries.