A full-cycle ERP built for pharmaceutical and homoeopathic manufacturers — supply chain, production, QC, and electronic Batch Manufacturing Record (BMR) in one auditable system. Already running in production at a licensed Bangladeshi manufacturer.
Pharmaceutical production carries a compliance burden that generic ERP or manual tracking wasn't built for. The gaps show up at audit time — or worse, on the production floor.
Raw material lot, QC approval, and production issue aren't linked — so tracing a finished batch back to its inputs takes hours, not seconds.
Hand-written batch records are slow to compile, hard to audit, and carry real risk of transcription mistakes during regulatory review.
Raw material, packing material, and finished goods sit in separate ledgers — nobody has one real-time view of what's actually on hand.
Retention samples and lab test results live outside the production record, making regulatory compliance reporting a manual scramble.
This is the exact module structure we built and deployed for a licensed homoeopathic manufacturer in Bangladesh — covering the full production cycle under GMP requirements.
We learn your production process, compliance needs, and current bottlenecks.
A walkthrough of the relevant modules against your actual workflow.
We see your floor firsthand — raw material intake, QC points, production lines.
Scoped modules, timeline, and cost based on what your operation actually needs.
Development, testing, staff training, and go-live — with ongoing support after.
This isn't a theoretical build — it's running production batches today at Maxfair & Company Ltd.
Modules are structured around the documentation and traceability regulators expect at audit time.
Based in Uttara, Dhaka — you talk to the people building your system, not a support queue.
Start with production & BMR, add sales, distribution, or HR modules when you need them.
"Excellent ERP solution for our manufacturing workflow."
Yes — the BMR module covers tablet, liquid, ointment, globules and mother tincture production with full recipe setup, material consumption, in-process control, and line clearance documentation.
Yes. Most clients start with Production, Raw Material, and BMR, then add Sales & Distribution or Retention Sample management as needed.
Yes — we visit your factory as part of the standard implementation process regardless of location within Bangladesh.
Timeline depends on module scope, confirmed after the factory visit and proposal stage — typically discussed in your free consultation.
Tell us how your production floor runs today — we'll show you what a GMP-compliant system looks like for it. No cost, no obligation.