This website is under development. Content, specifications and figures shown are placeholders for demonstration only — they are not accurate or genuine company information.
High-speed rotary tablet presses, automated capsule fillers, and sterile packaging machinery built to international WHO-GMP and 21 CFR Part 11 standards.
77 machines across 8 process categories, from single units to complete lines.
Wet and dry granulation equipment
9 machinesRotary, single punch & high-speed tablet compression machines
14 machinesFilm coating and sugar coating systems
9 machinesAutomatic, semi-automatic, and manual capsule filling machines
9 machinesLiquid filling, sealing, and processing lines
9 machinesAdvanced blister packaging for tablets and capsules
9 machinesBottle, vial, and container washing systems
9 machinesWFI, purified water, and plant utilities
9 machinesPrecision-engineered pharmaceutical machinery built to international GMP and WHO standards.
Showing 6 of 77
Machines are engineered to the standards your inspectors already work to, and shipped with the documentation that proves it.
Every stainless steel input is verified by spectrometer for chemical composition and delivered with mill test certificates (MTC 3.1).
Contact surfaces are mechanically and electro-chemically polished to a certified roughness, verified with calibrated profilometers.
Control architectures carry multi-tier access security, electronic signatures, time-stamped audit trails and automatic data archiving.
Headquartered in Kolkata with dedicated technical operations in Dhaka, GentlemanPharmed is a premier manufacturer and turnkey solution provider of pharmaceutical processing and packaging machinery.
We specialize in oral solid dosage (OSD) lines, sterile liquid injectables, and advanced automation retrofits. Every system we build integrates AISI 316L contact metallurgy, precision CNC tooling, and 21 CFR Part 11 compliant control architectures, backed by responsive on-site engineering support.

A machine is bought once and run for fifteen years. These are the four stages we stay involved through — from sizing the line to retrofitting it.
Before anything is built, the line is sized against what you need to produce.
Commissioning and the qualification evidence your auditors will ask for.
Keeping the line running once it is in production.
Bringing machines already on your floor up to current standards.
Pharmaceutical manufacturers across India, Bangladesh, and beyond rely on our machinery every day.
“We commissioned two RTP-35 Rotary Tablet Presses at our Gazipur manufacturing plant. The machines have delivered an exceptional 99.4% uptime across double-shift production, and the technical validation support from GentlemanPharmed was flawless.”
Engr. Tariqul Islam
VP Manufacturing Operations, BD Pharmaceuticals Ltd.
“The AF-150 automatic capsule filler has transformed our capsule dosing accuracy. Weight variation across our 500mg antibiotic lines dropped to under 1.1% RSD. Their Kolkata engineering center provides immediate spare parts support whenever needed.”
Sunil Verma
Plant Technical Director, Apex Lifesciences India
“GentlemanPharmed executed a complete 21 CFR Part 11 software and PLC upgrade on our existing blister packaging machines. The project was completed during our planned 7-day annual shutdown with zero startup delays.”
Dr. Arindam Sen
Head of Quality Assurance, Eastern Pharma Laboratories
“From pre-installation site surveys to IQ/OQ execution and operator training, their service engineers demonstrate deep pharmaceutical engineering expertise. A highly dependable equipment partner.”
Mahmudur Rahman
Chief Operating Officer, Savar Healthcare Formulations
“We took the layout and capacity study before committing to any equipment, and it changed what we bought. The throughput model accounted for changeover and cleaning rather than nameplate speed, so the line we installed actually hits the annual volume we planned it around.”
Priya Raghunathan
Director of Operations, Meridian Biotech
“Their validation team wrote and executed the cleaning validation protocols for a shared granulation train ahead of our EU-GMP inspection. The dossier held up under questioning without a single observation raised against it.”
Dr. Nasreen Akhter
Head of Regulatory Affairs, Northfield Formulations
Service response is the difference between a shift lost and a week lost. These are the offices your engineer travels from.
Everything you need to know about our pharmaceutical machinery.
Send us your output target, dosage form and any layout constraints, and our engineers will come back with a specification and quotation.