Pharmaceutical and biotech facilities require the highest standards of material purity, surface finish, and documentation. Clean steam systems, used for sterilisation (SIP), equipment cleaning (CIP), and humidification, demand SS 316L construction, electropolished surfaces, and full material traceability. AQ Process Systems sources and exports pharmaceutical-grade equipment meeting FDA, WHO GMP, and PIC/S standards.
In Indonesia, we supply pharmaceutical equipment to major manufacturers in Jakarta, Bandung, Semarang, and Surabaya, including Kalbe Farma, Sanbe Farma, Kimia Farma, Bio Farma (vaccine production), and multinational facilities. Indonesia's BPOM (Badan POM) regulatory alignment with WHO GMP standards is driving upgrades in clean steam and pure water systems across the sector.
In East Africa, we serve pharmaceutical manufacturers in Kenya (Nairobi, Cosmos, Universal, Beta Healthcare), Ethiopia (Addis Pharmaceutical Factory, Julphar Ethiopia), Tanzania, Uganda, and Rwanda. East Africa's growing local pharmaceutical manufacturing base, supported by WHO prequalification programmes and AfCFTA, is expanding demand for GMP-compliant clean steam equipment.
| Product Category | What We Supply |
|---|---|
| Diaphragm Valves | Sanitary diaphragm valves, SS 316L, electropolished, tri-clamp connections, EPDM/PTFE diaphragms, CIP/SIP capable. |
| Steam Traps | Clean steam traps, SS 316L construction, electropolished internals for autoclave and SIP condensate drainage. |
| Valves | SS 316L ball, butterfly, and check valves for clean steam distribution, pure water, and WFI (Water for Injection) systems. |
| Strainers | Sanitary strainers in SS 316L with tri-clamp connections and electropolished screens. |
| Boiler Spares | Electric clean steam generator components and plant utility boiler spares. |
| Condensate System Spares | Clean condensate return system components, SS piping fittings, sample coolers, conductivity sensors. |
Pharmaceutical manufacturers in Indonesia and East Africa face the dual challenge of meeting international GMP standards while managing procurement costs. European clean steam equipment is expensive and has long lead times. AQ Process Systems sources GMP-compliant equipment from quality manufacturers across India, Europe, and Japan, providing the same specifications and documentation at competitive pricing with shorter delivery times.
Yes. All pharmaceutical-grade equipment is supplied in SS 316L with Ra ≤ 0.8μm surface finish (or better), full material traceability (EN 10204 3.1), and documentation supporting WHO GMP, PIC/S, and FDA compliance. Tri-clamp (sanitary) connections are standard.
Yes. We supply to pharmaceutical facilities across Java, Jakarta, Bandung, Semarang, and Surabaya. We understand Indonesian BPOM requirements and supply equipment with appropriate documentation. Delivery via Jakarta is typically 10-14 days by sea.
Yes. We supply weir-type and zero dead-leg diaphragm valves specifically designed for CIP (Clean-in-Place) and SIP (Sterilise-in-Place), fully drainable, with FDA-compliant diaphragm materials and electropolished wetted surfaces. Available from 1/2" to 4".
Full material certificates (EN 10204 3.1 with positive material identification), surface finish reports (Ra measurement), weld logs (for welded assemblies), pressure test reports, dimensional reports, and certificates of conformity. All documentation is traceable to the individual batch or component.
Yes. We are actively supplying pharmaceutical equipment to facilities in Kenya, Ethiopia, Tanzania, and Uganda. Shipments via Mombasa or Dar es Salaam with full export documentation. We support WHO prequalification projects by ensuring all equipment meets the required standards and documentation.
Share your requirements, we respond within 24 hours with pricing and lead times for Indonesia & East Africa delivery.