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Your AI powered regulatory documentation workspace
Prepare, validate and manage your regulatory submissions faster with fewer errors and full compliance confidence.

For Pharma
DCE is designed for pharmaceutical manufacturers importers distributors and regulatory consultants who need faster approvals cleaner dossiers and full visibility into submission readiness.
From CTD compilation to final regulator review DCE acts as your digital regulatory officer guiding every step.
Get StartedInstant validation of document quality Automated error detection across CTD modules Downloadable correction and gap analysis reports
Guided CTD compilation from Module 1 to 5 Modular document organization by product and country Regulator ready dossier generation
Centralized secure document library Version control and full change tracking Project based organization by product and market
Submit with confidence in less time and fewer review cycles
AI powered validation catches issues before regulators do
Automated checks ensure nothing is missed across all CTD modules
All regulatory tools in one integrated platform
DCE eliminates these problems by embedding regulatory logic directly into your documentation process.
Most tools store documents. DCE understands regulatory structure logic and evidence
It does not just accept files It validates scientific consistency regulatory alignment and completeness
It is not a generic AI tool It is a purpose built regulatory decision support system
DCE is designed specifically for African regulatory environments while remaining fully aligned with global standards including ICH WHO and regional harmonization frameworks.
Whether you are submitting in Nigeria Ghana Kenya South Africa or expanding across multiple markets DCE scales with you.
Get StartedYour regulatory data is protected with strict access controls encryption and secure system architecture.
Higher first pass approval rates
Shorter regulatory timelines
Reduced regulatory spend
Improved documentation
Faster access to market
Better access to quality healthcare products
DCE is part of the ONBOARD regulatory technology ecosystem. This allows you to connect documentation compliance directly with automated workflows compliance alerts and product lifecycle tracking across multiple African markets.
You move from documentation to full market access execution in one platform.
Subscribe to our newsletter to stay informed about the latest regulatory updates, industry insights, and exclusive offers from Onboard.