Pharma & Hospital
Equipment.
GMP-compliant pharmaceutical machinery and hospital infrastructure — engineered with the precision, hygiene, and regulatory awareness that life sciences demand. Because every machine we build impacts human health.
Our Expertise
Solutions for Life Sciences & Healthcare
From tablet presses to operation theatres — every system engineered for regulatory compliance, patient safety, and validated performance.
Solid Dosage Manufacturing Equipment
Complete equipment lines for tablet and capsule manufacturing — from raw material milling through granulation, blending, compression, coating, and packaging. GMP-compliant machinery engineered for pharmaceutical-grade precision and validated performance.
Liquid & Semi-Solid Manufacturing
Manufacturing vessels, homogenizers, mixing systems, and filling lines for syrups, suspensions, solutions, creams, ointments, and gels. Hygienic design with CIP capability, jacketed heating/cooling, and validated process control.
Sterile & Injectable Equipment
Equipment and infrastructure for sterile pharmaceutical manufacturing — vial filling, ampoule lines, WFI systems, autoclaves, and depyrogenation tunnels. Engineered for aseptic conditions with RABS/isolator compatibility and 21 CFR Part 11 compliance.
Pharmaceutical Packaging Machinery
Primary and secondary packaging machinery for pharmaceutical products — blister packing, strip packing, bottle lines, cartoning, and serialization. High-speed, format-flexible machines with validation-ready documentation.
Clean Room & HVAC Systems
Pharmaceutical-grade clean rooms and HVAC systems designed, built, and validated for WHO-GMP, EU-GMP, and Schedule M compliance. Modular construction with integrated HEPA filtration, pressure cascade, and environmental monitoring.
Hospital & Healthcare Equipment
Specialized infrastructure for hospitals — medical gas pipeline systems, modular operation theatres, CSSD equipment, hospital furniture, and laboratory infrastructure. Engineered for patient safety, infection control, and clinical performance.
Nutraceutical & Veterinary Equipment
Manufacturing equipment for nutraceutical supplements and veterinary pharmaceuticals — sharing pharmaceutical-grade precision with formulation flexibility for diverse product formats, dosage sizes, and regulatory requirements.
What We Deliver
Pharmaceutical-Grade Engineering
GMP design, hygienic fabrication, validation documentation, and regulatory compliance — built into every machine.
GMP Design Engineering
Hygienic Fabrication
Validation Support
Automation & Controls
Regulatory Compliance
Service & Qualification
Industries Served by This Division
Trusted Across Multiple Sectors
Our Process
How We Deliver
A disciplined, proven approach tailored for this division — from first conversation to long-term support.
URS Review & GMP Assessment
We begin with your User Requirement Specification (URS), reviewing product formulation, batch sizes, regulatory requirements, and clean room classification to define equipment specifications.
Design Qualification (DQ)
Equipment design developed with GMP principles — contact material selection, surface finish specifications, CIP provisions, safety features, and control system architecture. DQ documentation provided.
GMP Fabrication
Fabrication in controlled environment with hygienic practices — mirror polishing, orbital welding where specified, crevice-free construction, and sanitary fitting integration.
Factory Acceptance Testing (FAT)
Comprehensive testing at our facility — operational verification, safety system checks, IQ protocol execution, and customer witness testing before dispatch.
Site Installation & Utility Connection
Equipment installation, leveling, utility connections (power, compressed air, water, steam), and clean room interface integration.
IQ/OQ Qualification
Installation Qualification and Operational Qualification protocol execution at site — verifying all parameters meet design specifications under installed conditions.
PQ Support & Handover
Support during Performance Qualification with your product — verifying consistent, repeatable performance. Complete documentation handover including operation manuals, spare parts lists, and maintenance schedules.
Frequently Asked Questions
Common Questions About
Pharma & Hospital Equipment
Are your machines GMP-compliant?
Yes. All pharmaceutical equipment is designed and manufactured in compliance with current Good Manufacturing Practice (cGMP) guidelines — including WHO-GMP, Schedule M, and EU-GMP requirements. Contact parts are SS316L with appropriate surface finishes, and designs incorporate CIP/SIP provisions.
Do you provide validation documentation?
Yes. We supply complete validation documentation including Design Qualification (DQ), Factory Acceptance Test (FAT) protocols, Installation Qualification (IQ) protocols, and Operational Qualification (OQ) protocols. We also support Performance Qualification (PQ) execution at your site.
Can your machines comply with 21 CFR Part 11?
Yes. Our control systems can be configured for 21 CFR Part 11 compliance — including electronic signatures, audit trails, user access management, and secure data recording. This is available as a standard or optional feature depending on the equipment.
What batch sizes can your equipment handle?
We supply equipment across the full scale — from laboratory/R&D (1-10 kg) to pilot scale (10-50 kg) to full production scale (50-1000+ kg per batch). Equipment is sized to match your current requirements with consideration for future capacity expansion.
Do you supply complete production lines or individual machines?
Both. We can supply individual machines (e.g., a single tablet press) or complete integrated production lines (e.g., granulation through packaging). For complete lines, we ensure inter-equipment compatibility, material flow optimization, and unified control architecture.
What hospital infrastructure do you supply?
We supply Medical Gas Pipeline Systems (MGPS), Modular Operation Theatres, CSSD (sterilization) equipment, stainless steel hospital furniture, laboratory infrastructure, and laundry management systems — all designed for patient safety and infection control compliance.
Do you supply to Ayurvedic and herbal product manufacturers?
Yes. We supply manufacturing equipment suitable for Ayurvedic, herbal, and traditional medicine production — with appropriate material compatibility, batch size flexibility, and compliance with AYUSH and related regulatory requirements.
What is the typical lead time for pharma equipment?
Standard equipment: 8-14 weeks. Custom equipment: 12-20 weeks. Complete production lines: 16-30 weeks. Timelines depend on specification complexity, validation requirements, and customization level.
Need GMP-Compliant Equipment?
Share your URS or product requirements — our pharma engineering team will design equipment that meets your regulatory, production, and validation needs.