Frequently Asked Questions
Know about us and what people asks about us
Who We Are?
MediHeaven Pharmaceutical Division is a global, end-to-end industrial solutions provider serving pharmaceutical manufacturers, biotechnology firms, R&D institutes, and healthcare organizations.
We bridge the gap between facility infrastructure engineering and daily commercial drug production. By consolidating seven core divisions—Process & Packaging Machinery, Raw Materials, Packaging Materials, Laboratory Instruments, Industrial Flooring, Cleanroom & HVAC Systems, and Process Utilities & Water Engineering—MediHeaven acts as a single-point strategic partner. From initial plant concept and cleanroom engineering to active pharmaceutical ingredient (API) sourcing and final packaging line validation, we deliver turnkey solutions built strictly to global cGMP, US FDA, WHO, and EU regulations.
Our Mission
To support and strengthen Bangladesh’s Pharma Industry, with the goal of making it globally competitive.
Our Vission
Developing strong partnerships by fulfilling expectations and honoring commitments.
Our Plan
Selectively partner with the best global brands to provide world class solutions to the local Pharmaceutical Industry.
Frequently Asked Questions
MediHeaven provides total pharmaceutical project execution and supply chain management across 7 dedicated divisions:
Process & Packaging Machinery
APIs, Excipients & Fine Chemicals (Raw Materials)
Primary & Secondary Packaging Materials
Analytical Laboratory Instruments
cGMP Industrial Flooring & Wall Systems
Modular Cleanrooms & HVAC Systems
High-Purity Water (PW/WFI) & Process Utilities
Yes. All our equipment, materials, cleanroom installations, and utility designs comply strictly with international authorities, including the US FDA, EU-GMP, WHO-GMP, PIC/S, and ISO standards (ISO 14644 & ISO 15378).
Yes. All processing equipment (tablet presses, granulators, liquid fillers) and packaging lines (blister packing, cartoning, serialization) are delivered with full validation documentation packages, including FAT, SAT, IQ, OQ, and PQ protocols compliant with 21 CFR Part 11.
Absolutely. Our secondary and tertiary packaging machinery accommodates hardware and software integration for 2D barcode printing, vision verification systems, and aggregation for global track-and-trace compliance.
Yes. Every batch of Active Pharmaceutical Ingredients (APIs), excipients, and functional additives supplied by our Raw Materials Division includes batch-specific COAs, MSDS, and DMF support for regulatory submissions.
We provide high-barrier primary packaging options including cold-form aluminum foil (Alu-Alu), high-grade PVC/PVDC films, Type I/II/III glass vials/ampoules, rubber stoppers, and desiccant-integrated container closures.
Our Industrial Flooring Division installs seamless, solvent-free epoxy coatings and thermal-shock-resistant Polyurethane (PU) concrete flooring. These systems eliminate microbial harbor points, resist harsh chemical cleaning agents, and handle heavy machinery traffic.
Our Process Utilities Division engineers Purified Water (PW) and Water for Injection (WFI) plants using multi-pass RO, EDI, and multi-effect distillation. Distribution loops are constructed with SS316L orbitally welded piping features zero-dead-leg valves, continuous TOC monitoring, and thermal sanitization routines.
