Pharmaceutical manufacturing
cGMP Process Equipment for Solid Dosage,
Liquid and Semi-Solid Pharmaceutical Manufacturing
Gansons has been manufacturing process equipment for the pharmaceutical industry since 1947. Today, more than 85% of our active installations operate in cGMP facilities regulated by the US-FDA, UK-MHRA, and European Medicines Agency (EMA) – making Gansons one of the most widely trusted pharmaceutical equipment manufacturers in the world.
cGMP Pharmaceutical Process Equipment. Designed for FDA, MHRA and EMA Regulated Facilities
We design and manufacture equipment for every critical unit operation in solid dosage form (OSD) manufacturing: from API blending and wet granulation through to drying, coating, particle sizing, and finished product powder transfer. Our equipment is engineered to minimise risk to product, personnel, and data — with hardware and automation architectures that support 21 CFR Part 11 compliance, GAMP 5, data integrity by design, and Pharma 4.0 integration.
Equipment for Every Stage of the Pharmaceutical Manufacturing Process
Gansons supplies pharmaceutical process equipment across the full OSD workflow and beyond:
Solid Dosage Granulation
The SuperGran® and High Shear Mixer Granulator are the core of our granulation offering. The inONE® R&D system combines granulation, drying and particle sizing in a single compact unit — ideal for formulation development and scale-up.
Tablet Coating
The GansCoater® is the world’s most advanced automated tablet coating system – and the highest-selling automated coater to US-FDA, EMA and UK-MHRA regulated pharmaceutical companies globally. Available from laboratory scale through to 1,500L production coaters, The GansCoater® delivers consistent, validated coating results with full data integrity and minimal operator intervention. It is the most specified automated coater for both film coating and functional coating of oral solid dosage forms.
Mixing and Blending
Powder Transfer and Material Handling
Contained material movement is critical in GMP pharmaceutical manufacturing – particularly for potent APIs, high-cytotoxic compounds, and segregation-sensitive blends. Gansons powder transfer solutions include vacuum transfer systems for closed-loop powder movement, IBC bin blenders for contained blending, and lifting and positioning devices for safe drum and container handling within GMP environments.
Particle Sizing
Cleaning Systems
Gansons Wash-In-Place (WIP) systems support rapid, validated cleaning of processing equipment without disassembly — reducing cleaning validation burden and operator exposure. Automated cleaning systems are available for granulators, fluid bed equipment, coaters, and powder transfer lines.
Automation and Control
- 21-CFR part 11 compliance for data integrity and storage, ALCOA+ compliant
- Pharma 4.0 enabled software, IoT enabled
- Smart graphs for lot reproducibility
- Responsive, ergonomic, intuitive interface
- 5 modes with multi-level password access
- Autonomous and Semi autonomous operations ready
Why Pharmaceutical Companies Choose Gansons
- Over 75 years of pharmaceutical equipment manufacturing heritage
- 85%+ of active installations in US-FDA, UK-MHRA and EMA regulated facilities
- India’s leading solid dosage form equipment manufacturer by market share
- In-house team of pharmacists, process technologists and validation engineers
- Innovation Centre in Thane available for proof-of-concept trials, scale-up studies and FAT
- Equipment designed for IQ/OQ/PQ, 21 CFR Part 11 compliance, GAMP 5 and data integrity by design
- Global installations across 40+ countries with local support through qualified agents