Industry fit · Pharma & chemicals
ERP software for pharma and chemical processing plants that begins with your own registers
Batch manufacturing records, in-process checks and deviation notes must be complete, signed and retrievable. Paper batch files are complete only until an inspector picks one at random.
What usually goes wrong
- Batch records assembled manually at the end
- In-process checks recorded without timestamps
- Deviations and rework poorly linked to batches
- Retest and expiry tracking on spreadsheets
The registers we digitise first
- Batch manufacturing and packing record
- In-process quality check sheet
- Deviation and change note
- Sampling and retest register
Same columns, same sequence as your existing sheet — filled on a phone, in the operator's language, with a photo of how to do each step.
What you can see from week one
- Batch-wise yield and cycle time
- Deviation count by stage
- Stock by batch with expiry
- Approved versus quarantined inventory
Ask for any of these in plain words and the assistant answers with the exact entries behind the number attached.
One record from order to dispatch
Every form entry moves through your approvals and your rules into stores, production, quality, maintenance, costing and dispatch — then into Tally through an agent on your own computer, so your books never leave your premises.