Taj Pharma India Ltd has emerged as a powerful name in the global pharmaceutical industry. Established with a vision to offer world-class healthcare solutions, Taj Pharma is headquartered in the industrious and strategically vital zone of Sarigam GIDC, Gujarat. This region, part of the Vapi-Daman industrial belt, is known for hosting some of India’s most prominent pharmaceutical and chemical manufacturing units.
With an unwavering commitment to quality, innovation, and regulatory compliance, Taj Pharma India Ltd has positioned itself as a reliable partner for international pharmaceutical companies seeking trustworthy manufacturing solutions, especially for regulated and semi-regulated markets. Let’s explore the world of Taj Pharma in depth, covering every facet of our operations, certifications, manufacturing capabilities, regulatory strengths, and global outreach.
Strategic Location in Sarigam GIDC – Heart of Pharma Manufacturing
The location of our headquarters and manufacturing facilities is not incidental. Sarigam GIDC is a part of the Vapi-Daman pharmaceutical hub, one of India’s most advanced and well-connected industrial regions. It offers:
- Proximity to Nhava Sheva (JNPT) and Mundra Ports for efficient exports
- Quick access to major cities like Mumbai, Surat, and Ahmedabad
- Availability of skilled technical manpower
- Strong logistics and infrastructure ecosystem
This strategic placement allows Taj Pharma to efficiently manage large-scale exports while maintaining regulatory compliance and timely product deliveries.
State-of-the-Art Manufacturing Facilities
At Taj Pharma, infrastructure is not just about physical space—it’s about intelligent design, regulatory alignment, scalability, and automation. Our manufacturing units are engineered with high-grade technology, following rigorous protocols as per WHO-GMP, PICS, and EU GMP guidelines.
We have dedicated cleanrooms, controlled environments, and modular production units that enable uninterrupted, contamination-free manufacturing of pharmaceuticals across various dosage forms.
Facility Highlights:
- Separate zones for OSD (Oral Solid Dosage), External Preparations, and Oral Liquids
- HVAC systems with HEPA filters for air handling
- Inline automated systems for blending, compression, encapsulation, and packing
- Integrated Quality Control (QC) and Microbiology labs
- EHS (Environmental, Health & Safety) compliant wastewater management
- 24×7 monitored data integrity and SCADA systems
This robust infrastructure ensures consistency in quality and efficiency at every step of production.
Certifications That Speak of Our Excellence
Taj Pharma India Ltd takes pride in the certifications and accreditations that validate our quality-centric approach. These include:
- WHO-GMP (World Health Organization – Good Manufacturing Practices)
Recognized globally, ensuring safety, efficacy, and quality in every product. - PICS (Pharmaceutical Inspection Co-operation Scheme) (Expected 2025)
Aligns Taj Pharma with the highest level of regulatory harmonization across over 50 countries. - EU-GMP (European Union – Good Manufacturing Practice) (Expected 2025)
Enables Taj Pharma to register and export pharmaceutical products to the regulated European markets. - ISO 9001:2018 Certified
Ensures robust quality management systems across all departments. - GLP (Good Laboratory Practice)
Guarantees accurate and reliable analytical and stability testing.
These certifications help Taj Pharma build strong trust with international clients, regulatory bodies, and healthcare providers.
Comprehensive Dosage Form Capabilities
Taj Pharma specializes in a diverse range of pharmaceutical formulations, designed to meet therapeutic needs across multiple segments. The dosage forms manufactured include:
1. Tablets – 120 Million Units/Month
Tablets are one of the most widely used dosage forms. Our tablet manufacturing line is capable of handling:
- Immediate-release
- Sustained-release
- Enteric-coated
- Bilayer tablets
- Multivitamins and therapeutic class drugs
2. Capsules – 40 Million Units/Month
From hard gelatin to HPMC vegetable capsules, our facilities cater to:
- Granule-filled capsules
- Pellet-filled capsules
- Powder-filled capsules
3. Dry Blended Powders / Granules – 36,000 kg/Month
Widely used in sachets and reconstitution-based medications, our powders meet precise particle size distribution and flow property requirements.
4. Effervescent Tablets – 20 Million Units/Month
We offer highly stable and moisture-resistant formulations, ideal for nutraceuticals and rehydration salts, with efficient tube or strip packaging.
5. Oral Jellies – 60 Million Units/Month
A fast-growing segment, especially for pediatric and geriatric applications. Our jellies are palatable, easy to administer, and available in various flavors and APIs.
6. Creams / Ointments – 40 Million Units/Month
We offer both water-based and oil-based external preparations:
- Antifungals
- Steroidal and non-steroidal formulations
- Dermatological creams
7. Oral Sachets – 3 Million Units/Month
Single-dose sachets used for probiotics, electrolytes, or antibiotics. Sealed with high precision for moisture protection and shelf-life stability.
End-to-End Regulatory Support for Global Clients
Taj Pharma does more than just manufacture medicines—we help our clients get them to market. Whether you’re seeking contract manufacturing, private labeling, or registration support, we provide end-to-end regulatory assistance.
Services Include:
- Dossier preparation in CTD/ACTD format
- Country-specific registration assistance (GCC, Africa, CIS, Latin America, EU)
- Product development and technology transfer
- Pharmacovigilance documentation and support
- Bioequivalence study support and documentation
We maintain a regulatory-ready archive of over 500 CTD-format dossiers for immediate product registration opportunities.
Robust Quality Assurance and Control
At Taj Pharma, every product passes through rigorous Quality Assurance (QA) and Quality Control (QC) procedures. Our dedicated teams operate independently of production to ensure complete objectivity and compliance.
Quality Control Highlights:
- Advanced HPLC, GC, UV, FTIR instruments
- Stability chambers as per ICH guidelines
- Microbiological lab for sterility, endotoxin, and microbial load testing
Quality Assurance Activities:
- In-process quality control (IPQC)
- Batch record review and release protocols
- Annual product quality review (APQR)
- Vendor audits and qualification
- CAPA, deviation management, and change control
Environmental and Social Responsibility
Taj Pharma follows sustainable manufacturing practices with a strong commitment to environmental safety. Our facilities are equipped with:
- Effluent Treatment Plants (ETP)
- Zero Liquid Discharge (ZLD) systems
- Solar power integration in operations
- Eco-friendly packaging and raw material sourcing
We also contribute to healthcare education, rural health camps, and disaster relief efforts as part of our corporate social responsibility.
Global Market Presence
Taj Pharma products are exported to over 42 countries, including:
- EU (upon EU-GMP approval)
- South-East Asia
- Middle East (GCC)
- Africa
- Latin America
- Central Asia & CIS countries
Our clients include government procurement agencies, global pharmaceutical chains, hospitals, wholesalers, and institutional buyers. We understand the compliance demands of each territory and deliver accordingly.
Why Global Clients Choose Taj Pharma
- ✅ WHO-GMP, EU-GMP, PICS Compliant
- ✅ High-volume, diversified dosage manufacturing
- ✅ Fully automated and regulatory-aligned infrastructure
- ✅ Fast turnaround for custom formulations
- ✅ Ready dossiers for rapid market registration
- ✅ Ethical, transparent, and partnership-driven approach
More Than a Manufacturer – A Strategic Partner
Taj Pharma India Ltd is more than a pharmaceutical manufacturer—we are a reliable, forward-looking partner committed to delivering superior healthcare solutions. Whether you’re looking for a long-term manufacturing ally, a regulatory expert for new market entry, or a supplier for high-quality generics, Taj Pharma offers the infrastructure, expertise, and trust you need.
As India continues to lead the way in global generics, Taj Pharma remains at the forefront—driving quality, affordability, and innovation in every formulation.
Get in Touch with Us Today
📞 Call: +91 84484 44095
📱 WhatsApp: +91 7400009975 / +91 7400009976
📧 Email: info@tajpharma.com
🌐 Website: www.tajpharmaindia.com
🏭 Manufacturing Address:
Taj Pharma India Ltd.
Plot No. 1019, Sarigam GIDC, Road No. 10,
District Valsad, Gujarat – 396155, India
Certifications: WHO-GMP, ISO 9001:2018, GLP, (EU GMP & PICS)
Taj Pharma India Ltd is a premier WHO-GMP certified pharmaceutical manufacturer based in Sarigam GIDC, Gujarat, India. With advanced facilities and a monthly production capacity of 120 million tablets and 40 million capsules, the company is poised to achieve PICS and EU GMP certifications, further expanding its global reach. Taj Pharma specializes in a wide range of dosage forms, including tablets, capsules, creams, ointments, oral jellies, effervescent tablets, and sachets. The company provides complete regulatory support for product registration and import manufacturing across regulated and semi-regulated markets. Taj Pharma exports to over 40 countries and operates with strict adherence to international quality and safety standards. With a strong infrastructure and a focus on innovation, Taj Pharma is a trusted partner for global pharmaceutical companies looking for reliable, high-quality, and affordable healthcare solutions. Choose Taj Pharma—where quality meets global healthcare excellence.
