Use case

RIMS for generic crop-protection companies

Generic crop-protection companies face unique regulatory challenges: managing data-matching packages, equivalence assessments, bridging studies, and multi-market submissions — often across dozens of active substances and hundreds of formulated products. Coveroff was built for exactly this workflow.

The challenges generic companies face

If your regulatory team recognises any of these, you're not alone.

Dossiers scattered across SharePoint and email

Studies, endpoints, and GAP tables buried in Word docs and spreadsheets. Data-matching evidence spread across folders with no single source of truth.

Multi-market registrations tracked manually

Your team manages registrations across EU zones, EPA, ANVISA, UK CRD, and PMRA — but the tracking lives in Excel with no real-time visibility.

Equivalence and bridging data disconnected

Active substance equivalence assessments, bridging studies, and source-of-supply documentation exist in separate silos, making cross-referencing manual and error-prone.

How Coveroff solves this

A data-native RIMS designed from the ground up for agrochemical regulatory science — not retrofitted from pharma or generic project management.

Structured regulatory data, not documents

Every study, endpoint, MRL, and obligation is a queryable record. Your regulatory data is structured and interconnected — not locked inside PDFs and Word files.

EU Reg 283/2013 & 284/2013 templates built in

Start with pre-built dossier templates that match EU regulatory requirements. Track completion per section and identify gaps before submission deadlines.

One formulation, every regulatory format

Define your formulation data once and render it for EU zonal, EPA, ANVISA, UK CRD, or PMRA formats automatically. No duplicate data entry across markets.

AI agents that understand your data

Connect AI agents via MCP server and REST API. They draft sections, flag gaps, and cross-reference studies using real structured data — no document parsing needed.

Built-in support for every major regulatory framework

EU Reg 283/2013EU Reg 284/2013EU Zonal (North / Centre / South)US EPAANVISA (Brazil)UK CRDPMRA (Canada)

Define your formulation and active substance data once. Coveroff renders it into every regulatory format your markets require — no manual reformatting, no duplicate spreadsheets.

Ready to replace spreadsheets?

Book a 30-minute demo and we'll walk you through Coveroff using your own portfolio. No slides, no pressure.