cGMP & GMP Certified Equipment

💊 Pharmaceutical Industry

Custom-fabricated cGMP and GMP certified industrial equipment for API synthesis, formulation, sterile manufacturing and packaging. Compliant with Schedule M, WHO-GMP, EU-GMP and 21 CFR Part 211.

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Equipment for Pharmaceutical Manufacturing

Machineries India is a trusted supplier of cGMP-certified industrial equipment for India's pharmaceutical industry. We supply equipment for the complete pharmaceutical manufacturing chain — from raw material storage and API synthesis to granulation, drying and formulation. All equipment is manufactured to Schedule M (Drugs & Cosmetics Act), WHO-GMP, EU-GMP and customer-specific URS.

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cGMP Pressure Vessels
SS 316L jacketed vessels with Ra ≤ 0.4µm electropolished interiors for API synthesis and bulk drug manufacturing.
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Pharma Grade Storage Tanks
cGMP SS 316L storage tanks with CIP/SIP nozzles, electropolished finish and full validation documentation.
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Ribbon Blenders & Mixers
GMP ribbon blenders, high-shear mixers and planetary mixers for dry powder blending, wet granulation and cream manufacturing.
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Jacketed Reactors
cGMP-grade jacketed batch reactors and glass-lined reactors for API synthesis and pharmaceutical intermediates.
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Fluidised Bed Dryers (FBD)
cGMP FBDs with SCADA control, HEPA filtration and full DQ/IQ/OQ/PQ validation documentation.
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Cartridge & Nutsche Filters
Liquid filtration cartridge housings and ANFDs for API recovery and pharmaceutical intermediates.
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Why Machineries India for Pharmaceutical Industry?

With 10+ years of experience supplying equipment to the Pharmaceutical Industry, we understand the unique process, compliance and material requirements of your manufacturing operations. Our in-house design engineers work closely with your team to select the right equipment type, material of construction, surface finish and certifications for your specific application.

All equipment is fabricated at our modern facility with qualified welders (WPS/PQR certified), CNC fabrication and rigorous quality control. We provide complete documentation including material test certificates, inspection records, performance test data and all compliance certificates required for your plant approval.

Compliance & Certifications

We ensure your equipment meets all applicable Indian and international standards so you can focus on production without regulatory concerns.

Frequently Asked Questions

cGMP (current Good Manufacturing Practice) for equipment means the vessel or machine is manufactured with no dead zones, SS 316L contact parts, smooth welds (Ra ≤ 0.8µm or better), easy-to-clean design, and is supplied with complete documentation including material certificates, surface roughness measurements, and validation protocols (DQ/IQ/OQ/PQ).
Yes. All pharmaceutical equipment is supplied with material test certificates (EN 10204 3.1), surface finish measurement reports, hydro test certificates, weld inspection records, and validation documentation as required by Schedule M of the Drugs and Cosmetics Act, India.
We offer Ra ≤ 0.4µm electropolished (EP), Ra ≤ 0.8µm mechanically polished (MP), and Ra ≤ 1.6µm mechanically polished for different application requirements. EP finish is standard for API vessels and sterile manufacturing.

Need Equipment for Pharmaceutical Industry?

Share your specifications and compliance requirements. Our engineering team responds within 48 hours.

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