If you’re seeking a fully compliant sterile injectable manufacturing plant in the Baddi pharmaceutical hub, this opportunity might be exactly what you’re looking for. The facility is, an ISO-certified, WHO-GMP-approved pharmaceutical company, is offering its Injectable Pharma Plant for Sale in Baddi. This facility is ideal for businesses aiming to manufacture sterile dry powder injections, sterile liquid injections, and ophthalmic products. It is one of the top destination for third-party manufacturing seekers in the region.
Highlights of the Facility
| Parameter | Details |
|---|---|
| Location | Baddi, District Solan, Himachal Pradesh |
| Established In | 2005 (Construction Started Feb 2004) |
| Certifications | WHO-GMP, GMP, GLP, ISO Certified |
| Licensed For | SVP (Liquid Vials, Ampoules), Dry Powder Injections, Ophthalmic Preparations |
| Facility Type | Sterile General + Beta Section |
| Total Site Area | 40,000 sq. ft. |
| Built-up Area | 15,000 sq. ft. x 4 floors |
| Working Days | 6 Days/Week (9:00 AM – 5:30 PM) |
| Manpower | more than 100 Trained Employees |
Injectable Pharma Plant for Sale in Baddi: Licenses
This Pharma Company is licensed by the Food and Drugs Control Administration, Himachal Pradesh, under Form 25 & 28 to manufacture:
- Small Volume Parenterals (SVP) – Liquid vials, ampoules, dry powder injections
- Sterile Ophthalmic Preparations
- Beta Lactam Injectables – Dry Powder
Export Ready:
The Pharma company is ready to export anywhere in the world with a neutral code – HP/Drugs/MNB/****** & HP/Drugs/1VB/******. The company is count among the top company in the region.
WHO-GMP Certified Quality Management System Functional
This facility is built and operated under strict cGMP protocols with regular audits and validations. Core QMS features include:
- Written SOPs & protocols
- Self-inspections (twice a year)
- Batch record reviews
- Vendor audits and qualified vendor list
- Complaint handling & product recall system
- Comprehensive training programs for all technical personnel
Quality Motto of the Company:
“Innovation and Quality Culture, Customer Satisfaction, Employee Empowerment through cGMP and GLP.”
Personnel & Hygiene Protocols
- GMP-compliant gowning areas (separate for male/female)
- Lint-free garments for sterile areas
- SOPs with photo-guided gowning and hand-washing procedures
- In-house & external training programs with feedback-based evaluations
- Yearly medical checkups & vision tests for visual inspection personnel
Details of Facility Infrastructure & Utilities
Air Handling Units (AHUs)
- 23 AHUs (12 dedicated for Beta Section)
- HEPA terminal filters (0.3 micron)
- RH Control (NMT 25% in dry areas, NMT 55% in non-critical)
- 60+ air changes per hour
Water Systems
- Purified Water & WFI System: Fully looped, validated, 24/7 recirculating loop (WFI at NLT 80°C)
- Stainless Steel Tanks, Dead Leg Ratio < 1.5x ID
- RO + Distillation based system with validated sampling protocols
Effluent Treatment Plant (ETP)
- Capacity: 88 KL/day trade effluent + 25 KL/day non-trade
- Parameters compliant with CPCB guidelines
Equipment & Automation in place
All production and QC equipment follow validation, calibration, and preventive maintenance protocols. Equipment highlights include:
- Contact parts: SS316L
- Automated material & batch handling via PLCs
- Microprocessor-based manufacturing systems
- Digital inventory and lab systems
- Daily manufacturing records are updated digitaly every day
Validation & Calibration are followed strictly
- Validation Master Plan (VMP) for all facility and process validations
- Area, Process, Cleaning, Equipment, Analytical validations performed
- Routine revalidation for any change control
- External & Internal Calibration Logs maintained for:
- Balances, Thermometers, Pressure Gauges, etc.
Cleaning & Maintenance As Per WHO-GMP
- Areas categorized as per WHO-GMP norms (e.g., Production, Warehouse, QC, Utility)
- Validated cleaning SOPs and checklists
- Dedicated preventive maintenance program
- Logs maintained as per FDA audit expectations
- Ready for any inspection every day
Why This Plant Is a Smart Investment
This is a rare opportunity to acquire a ready-to-operate sterile manufacturing unit in India’s premier pharmaceutical zone. Whether you’re a contract manufacturing company, an expanding PCD brand, or a global buyer looking for an export-compliant facility — this setup gives you everything.
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FAQs
What dosage forms are licensed for this plant?
Liquid injections, dry powder injections, ampoules, and ophthalmic preparations.
Can this facility export to regulated markets?
Yes, it holds a neutral code and WHO-GMP certification, making it export-ready.
Are Beta and General sections separate?
Yes, separate areas and AHUs are maintained for Beta Lactam section.
What is the manpower strength?
Around 100 trained employees are working across departments.
What cost may occur for setup a new similar plant?
The actual cost may differ due to various factors but with similar set of machinery and sections. It would be around INR 35 crore, and will take 3 years in establishment process.
Final Thoughts for this Facility
With its perfect compliance track record, robust infrastructure, and strategic location[Baddi], This Pharma Company’s sterile injectable facility in Baddi is a high-value acquisition for any pharmaceutical entrepreneur or investor. While analyzing by putting my 23 years experience in this field I can easily say it is a perfect and tension free manufacturing facility that offers a great client base with more than 6 crore per month sale.
