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eDocument Management

Every attachment findable, none of it slowing the system down

Regulated manufacturing generates an enormous volume of scanned documents — COAs from suppliers, invoices, licences, certificates. Holding them in the transactional database makes the system slow. DeepPharmaERP keeps them in a separate repository, indexed and linked, with no impact on transaction performance.

Repository
Supplier COAs
4,182
Invoices
9,640
Licences
126
Expiring soon
7
Capabilities

What eDocument Management covers

Repository

  • Image and PDF upload against any transaction or master
  • Separate storage layer with zero impact on the transactional system
  • User-defined document types with mandatory and optional rules

Retrieval and control

  • Retrieval from the record it belongs to, not by folder hunting
  • Missing document reporting against expected document checklists
  • Version control and retention rules per document type
AI in this module

What the system notices for you

Suggestions only. Nothing here signs, approves or dispositions anything — a qualified person decides and the audit trail records who. Every model shows the data behind its suggestion, and every feature can be switched off per site.

DeepPharma AI

Automatic classification

Reads an uploaded document and proposes its type, the record it belongs to and its expiry date.

DeepPharma AI

Data extraction

Pulls values from supplier COAs and invoices for verification instead of manual entry.

DeepPharma AI

Expiry monitoring

Watches licences, certificates and qualification documents and warns before they lapse.

How the AI works across the plant
Questions

eDocument Management — common questions

Will storing scanned documents slow the system down?

No. Documents live in a separate repository rather than in the transactional database, which is the design decision that keeps a system with years of scanned COAs responsive.

Can the system tell me what is missing?

Yes. Expected-document checklists per record type drive a missing document report, and licence and certificate expiry dates are monitored with advance warning.

See it on your own floor.

Two hours with your production and QA leads. We walk one product end to end and show you where it lands in the system — then you decide whether a gap study is worth it.