Plant listing · Baddi, Himachal Pradesh
Sterile Injectable Pharma Plant for Sale in Baddi
A WHO-GMP-certified sterile manufacturing facility in Baddi, District Solan, licensed for liquid vials, ampoules, dry powder injections and ophthalmic preparations.
At a glance
Facility overview
The plant was established in 2005, with construction started in February 2004. It has a sterile general section and a Beta section, and operates six days per week from 9:00 AM to 5:30 PM.
| Parameter | Details |
|---|---|
| Location | Baddi, District Solan, Himachal Pradesh |
| Certifications | WHO-GMP, GMP, GLP, ISO Certified |
| Licensed for | SVP (Liquid Vials, Ampoules), Dry Powder Injections, Ophthalmic Preparations |
| Facility type | Sterile General + Beta Section |
| Built-up area | 15,000 sq. ft. × 4 floors |
| Manpower | More than 100 trained employees |
Licensed scope
Injectable and ophthalmic manufacturing
Dosage forms
- Small Volume Parenterals (SVP): liquid vials, ampoules and dry powder injections
- Sterile ophthalmic preparations
- Beta Lactam injectables: dry powder
Licensing and export status
The company is licensed by the Food and Drugs Control Administration, Himachal Pradesh, under Form 25 & 28. It is described as export-ready with neutral codes HP/Drugs/MNB/****** and HP/Drugs/1VB/******.
Quality systems
cGMP operations and validation
Quality management system
Documented controls
Quality processes are presented against CDSCO expectations and the facility’s stated WHO-GMP and GLP practices.
- Written SOPs and protocols
- Self-inspections twice a year
- Batch record reviews
- Vendor audits and qualified vendor list
- Complaint handling and product recall system
- Training programs for technical personnel
Validation and calibration
Planned, recorded processes
For a broader readiness review, see Laafon’s CDSCO Schedule-M Compliance Dashboard.
- Validation Master Plan for facility and process validations
- Area, process, cleaning, equipment and analytical validations
- Routine revalidation under change control
- External and internal calibration logs for balances, thermometers and pressure gauges
- Daily manufacturing records updated digitally
“Innovation and Quality Culture, Customer Satisfaction, Employee Empowerment through cGMP and GLP.”
Infrastructure and utilities
Sterile production support systems
Air handling and hygiene
- 23 AHUs, including 12 dedicated to the Beta Section
- HEPA terminal filters rated at 0.3 micron
- RH control: NMT 25% in dry areas; NMT 55% in non-critical areas
- 60+ air changes per hour
- Separate male and female GMP-compliant gowning areas, lint-free garments and photo-guided gowning and hand-washing SOPs
- Yearly medical checkups and vision tests for visual inspection personnel
Water, effluent and equipment
- Purified Water and WFI: fully looped, validated, 24/7 recirculating loop; WFI at NLT 80°C
- Stainless steel tanks; dead leg ratio below 1.5× ID
- RO + distillation system with validated sampling protocols
- ETP: 88 KL/day trade effluent + 25 KL/day non-trade; stated CPCB compliance
- SS316L contact parts, PLC batch handling, microprocessor-based manufacturing, and digital inventory and lab systems
Buyer context
A ready-operating plant in the Baddi pharma hub
This listing may suit third-party manufacturers, expanding PCD brands and buyers seeking an export-ready sterile manufacturing setup in Baddi. Production, warehouse, QC and utility areas are stated to be categorized to WHO-GMP norms, with cleaning SOPs, checklists and preventive maintenance records maintained to FDA audit expectations.
Important: The INR 35 crore / 3-year comparison and ₹6 crore+ monthly sales are seller-provided figures. They are not an independent valuation, forecast, legal opinion or financial advice. Verify licences, inspection history, machinery, financials, customer base, capacity and all regulatory claims through due diligence before any commitment.
For a separate planning estimate, use the Pharma Plant Setup Cost Calculator. You can also review other pharma plants for sale on Laafon.
FAQs
Questions buyers commonly ask
Darshan Singh
Founder, Laafon Galaxy Pharmaceuticals · 23 years in pharmaceutical QA/QC & drug regulatory affairs.
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Listing information, capacities, certifications, availability and commercial figures are supplied for enquiry purposes and should be independently verified. This content is not legal, regulatory, investment or financial advice.
