By Industry · Food & Biotech Sample content

Compliance & Traceability for Food and Biotech

Lot traceability, shelf-life control, and GMP / HACCP compliance in one go.

100%
Lot traceability
0
Audit findings
−80%
Recall cost
PAIN POINTS

This happens every single day

Lot tracking is a mess

One raw-material lot ends up in 20 finished products — and tracing a problem takes a week.

Shelf life is hard to manage

Near-expiry stock piles up while a part-timer checks it cell by cell in Excel every day.

Preparing for GMP audits

The whole company scrambles for a week before an audit, chasing document versions everywhere.

Recalls trace too slowly

A contaminated ingredient forces a recall, and tracing back from finished goods takes 3 days.

RECOMMENDED MODULES

The modules we recommend for you

Each module is tuned to your scenario — run one on its own, or combine them.

ERP

Ingredients, formulas and production orders in one system, with GMP document control.

MES

Process lots linked automatically, with live temperature and humidity records.

See the module

Labeling

One code per item, tracing from raw material to finished product.

SCENARIOS

Three typical scenarios

01

Forward and backward lot tracing

When a raw-material lot goes bad, find every affected finished-goods lot in 30 seconds.

  • Raw material to process to finished goods, end to end
  • Trace both forward and backward
  • Look up any customer lot in one click
02

FEFO shelf-life management

The system sequences shipments by expiry date and flags near-expiry stock automatically.

  • Automatic FEFO issuing
  • Alerts at 30/60/90 days to expiry
  • Write-off losses down 70%
03

Paperless GMP documentation

Batch records, SOPs and calibration logs all go electronic — the auditor just opens a screen.

  • Batch records captured electronically in real time
  • Full document version control
  • Auditors can review remotely
FAQ

FAQ

We are a traditional-medicine plant with special regulations — does this work for us?

We already serve traditional-medicine, pharmaceutical, food and supplement manufacturers, with formulas and processes customized to each.

Will auditors accept electronic GMP records?

The system meets FDA 21 CFR Part 11 and PIC/S electronic-signature requirements, and multiple customers have passed audits with it.

Do you support temperature and humidity monitoring?

MES connects to temperature and humidity sensors, logging in real time and alerting on any excursion.

Do our ingredient suppliers need to run this too?

No — the SCM module simply lets suppliers upload their COAs.

Ready to get started?

Book a 30-minute consultation — we will shape the module mix around your Food & Biotech needs.

Book a consultation