Pharma & Life Sciences
Regulatory Submission Compilation
Compile eCTD submissions by gathering documents from legacy DMS and assembling per regulatory requirements.
Regulatory DMSIn Production
How It Works
1
Pull document lists from the submission plan
2
Retrieve approved documents from the document management system
3
Validate document formats, hyperlinks, and metadata
4
Assemble the eCTD structure and perform technical validation
What This Enables
Reduces eCTD compilation time from weeks to days
Eliminates technical validation errors that cause rejection
Handles the complexity of multi-regional submissions
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Customers go from zero to production in 3 weeks. See how Minicor can automate this workflow for your EHR.
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