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Specialist software. Pharmacy first.
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Wholesalers & quality teams

Follow the batch—not just the stock total.

A quantity on screen does not explain whether a batch can be supplied. A useful demonstration follows receipt, quality status, allocation and dispatch, then shows what happens when one of those steps cannot proceed.

By the Pharmix product team · Reviewed
Follow the handover
  1. 01Receive & identify
  2. 02Hold & review
  3. 03Release & pick
  4. 04Dispatch & trace

Illustrative process—not live patient data or a clinical decision tool.

01

Separate physical receipt from availability

A received batch may still need review. Demonstrate a hold, the role permitted to release it and the history retained after the decision. The software's record supports your quality system; it does not issue a wholesale licence or certify GDP compliance.

  • Product, pack, batch and expiry captured
  • Held stock excluded from saleable availability
  • Independent authority and reason recorded
02

FEFO needs rules and exceptions

First-expiry-first-out is a stock selection approach, not permission to supply every short-dated item. Review configured pre-expiry blocks, customer requirements, shortages and alternative batches. A wrong scan or a partially picked order needs a visible resolution path.

  • Available versus held or allocated stock
  • Wrong-batch and shortage scenarios
  • Customer packing and mixing rules
03

Close the trace at dispatch and return

Connect the picked batch with its load, customer documents and delivery evidence. For a return, show how the original supply is identified and how the quality decision is kept separate from putting goods back into available stock. Repacking has its own material-balance and release records.

  • Batch-to-customer movement history
  • Returns and discrepancy reasons
  • Repacking artwork, material balance and review
Make it specific

Bring one real workflow. Leave the patient details out.

Use de-identified examples to agree product fit, configuration, responsibilities and acceptance criteria. This guide is software procurement information, not clinical or regulatory advice.

Discuss your requirementsExplore the related product
Further reading

MHRA: good manufacturing and distribution practice. This independent reference provides background, not endorsement or certification of Pharmix. Local procedures and professional responsibilities remain with your organisation.

Start with your workflow

A clearer next step for your pharmacy.

Discuss your team, stock journey or medicines data with the people building the software.

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