Park Pharmaceuticals provides reliable, compliant, and cost-effective third-party manufacturing for pharmaceutical companies of all sizes. With modern facilities, validated equipment, and an
experienced team, we deliver consistent production and complete documentation support for every batch.
Our goal is simple: to make manufacturing seamless while maintaining strong process control, regulatory compliance, and timely delivery. As a WHO-GMP and GLP-certified manufacturer, we ensure quality and consistency from start to finish.
Our Licensed Manufacturing Capabilities
- Beta-lactam & Non-Beta-lactam formulations
- Cephalosporin products
- Sustained Release, Film-Coated, Uncoated, Chewable, Tablets
- Capsules
- Injectables (Dry & Liquid forms)
- Oral Suspensions & Syrups
- Ready-to-compress granules and ready-to-fill powders for various applications
- Ophthalmic preparations.
Client Engagement: Share your product idea, quantity, and specifications.
Product Formulation & Specification: Our R&D and production teams configure the process as per your requirements.
Regulatory Compliance: Full compliance with Indian and global regulatory norms.
Raw Material Procurement: Only certified suppliers are used for APIs and excipients.
Production: Controlled blending, granulation, filling, encapsulation, or tableting using validated systems.
Quality Assurance: In-process testing for purity, potency, dissolution, and stability.
Packaging: Customized packaging to meet regulatory and commercial needs.
Documentation: Complete batch documentation for audits and submissions.
Delivery: Safe and timely delivery to your chosen point.
Regulatory Filing Assistance: Support for dossiers and regulatory filings when required.
Cost Efficiency: Reduce investment and benefit from our large-scale operations.
Focus on Core Competencies: We handle manufacturing while you focus on your brand.
Quality Assurance: Strong GMP/GLP systems and validated testing protocols.
Scalability: Increase or reduce production as needed with no extra infrastructure cost.
Faster Time-to-Market: Quick setup using our ready infrastructure.
Risk Mitigation: Multiple validated lines and cross-trained teams ensure continuity.
Specialized Expertise: Experience across tablets, capsules, syrups, liquids, and injectables.
Global Regulatory Support: Assistance for Indian and export markets.
Transparent Costing: Clear pricing and agreements.
International Reach: Serving partners across Asia, Africa, the Middle East, CIS, and Latin America.
Infrastructure Savings: No need to invest in new facilities.
Customization: Tailored production for every product and market.
Companies partnering with Park Pharmaceuticals must provide:
Drug License
GST Certificate
Quality Control Documents
Manufacturing Agreement
Any additional regulatory documents needed for your product or market
What is Third Party Manufacturing?
Outsourcing production to a specialized manufacturer like Park Pharmaceuticals, who manages formulation, production, testing, packaging, and compliance.
Key Benefits?
Cost savings, faster launches, consistent quality, and zero infrastructure investment.
How is product quality ensured?
Each batch undergoes in-process checks, validated testing, and final QA before release.
Which products can be manufactured?
Tablets, capsules, syrups, dry syrups, injectables, ophthalmic formulations, and more.
What documents are needed?
Drug license, GST certificate, QC documents, manufacturing agreement, and market-specific regulatory files.
Ready to streamline and scale your pharmaceutical production?
Our team can support you through every stage.