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SITE 01 · Shendra MIDC

Shendra API and OSD

Our flagship integrated campus: 14 blocks, of which 9 are dedicated to API manufacturing through 17 clean room modules, with capability for hydrogenation and cryogenic reactions. The fully automated Metformin HCl block runs on a DCS system with state-of-the-art powder transfer, supported by five purified-water systems, one WFI system and a QC laboratory with the latest instrumentation. The campus also houses a state-of-the-art oral finished dosage facility and operates as a zero liquid discharge site.

INSPECTED & APPROVED BY

USFDA (USA) · PMDA (Japan) · MFDS (Korea) · ANVISA (Brazil) · COFEPRIS (Mexico) · German Health Authority, BGV · NCPHP (Hungary) · WHO-GMP · CDSCO & FDA Maharashtra (India)

175,645 m²
TOTAL PLOT AREA
1,650 KL
Installed Capacity
+1,540 m²
PROPOSED EXPANSION
SITE 02 · Shendra MIDC

Shendra B6 Plant

Our newest site, currently under construction: two plants with a dedicated purified-water system and a zero-liquid-discharge waste treatment plant, designed for products such as Dextromethorphan HBr with vertical gravity process flow.

33,120 m²
TOTAL PLOT AREA
450 KL
Volumetric Capacity
SITE 03 · Chikalthana MIDC

Chikalthana E9 Plant

Thirteen plants across plots E-7, E-8 and E-9 with two purified-water systems and a waste treatment plant, including dedicated Metformin HCl and Riboflavin Phosphate Sodium plants with vertical gravity process flow.

30,581 m²
PLOT AREA (E-7/8/9)
302 KL
Installed Capacity
14,980 m²
PLOT AREA (E-53)
SITE 04 · Shendra MIDC

FDF Plant

A dedicated finished dosage facility for oral solid dosage forms, tablets and capsules, and directly compressible (DC) granules, with capacity expanding to 10.00 billion units per annum. All processing areas, corridors, primary packing, dispensing and sampling areas are built to Class 100,000 / Class D / ISO 8 standards with 0.3µ terminal HEPA filters and a dedicated AHU per processing area, with separate personnel and material airlocks and access control for critical areas.

Purified water is generated at 2,000 L/hr through two-pass RO with EDI, and operations run on SAP S/4HANA with Caliber QAMS and LIMS. Accredited by USFDA (USA), NIPN Hungary (EU), WHO-GMP by CDSCO & FDA Maharashtra (India) and ZAZIBONA (Southern Africa).

40,000 m²
Total Plot Area
6.70 Bn
Units Per Annum
2,345 TPA
DC Granules
INFRASTRUCTURE & DESIGN

Engineered for Contamination-Free Production

Every zone is designed to cGMP requirements, from building structure to airflow, for manufacturing, packaging, testing and release. Expand each principle to see how it’s engineered.

NEXT STEP

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Four manufacturing facilities engineered to global cGMP standards, supplying regulated markets worldwide.
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