Solutions for pharmaceutical plants
Faster release, audit-ready microbiology and validated filtration for pharma and API plants in Bangladesh. We supply the instruments and filters, and our engineers install, qualify and service them.
The pressures pharma QC faces
- Batch release waits on micro results that take days.
- Audits by DGDA and, for export plants, US FDA, EU and WHO inspectors expect complete, traceable data.
- EM and OOS investigations need fast, species-level answers.
- Filtration must be correctly rated and documented for every step.
How we help
| Need | Solution | Products |
|---|---|---|
| Faster micro results, shorter quarantine | Rapid Microbial Testing | Microbs IAN — counts in 15 minutes, 21 CFR Part 11 |
| Identify EM and OOS isolates | Microbial Identification | Autobio Autof MALDI-TOF series |
| Sterile and process filtration | Filtration | Global Filter cartridges, 0.2 µm to prefilter, housings |
| Everyday lab supplies | Lab consumables | Culture media, MAT, BI/CI, disinfectants, data loggers |
For export-oriented plants
If you supply regulated export markets, data integrity and a documented validation path matter most. IAN’s 21 CFR Part 11 compliance, on-site IQ/OQ/PQ by our engineers and manufacturer documentation give your QA team what auditors ask for.
For plants growing in the local market
As volumes grow, QC capacity becomes the bottleneck. In-house MALDI-TOF identification and pharma-grade filters with local supply help you keep pace without adding delay.
Local support
Installation, IQ/OQ/PQ executed by our engineers, training and AMC, from our Dhaka team, across Bangladesh.
FAQ
Can you help with validation documents?
Yes. Protocols come from the principal or Pharma Biotech, and our engineers execute them on site.
Do you work with plants outside Dhaka?
Yes, our engineers travel across Bangladesh.
Tell us what your lab needs
An engineer replies with a recommendation and a quote.