Third Party Manufacturer For Pharma
Third Party Manufacturer For Pharma Specification
- Shelf Life
- 24 Months
- Effect
- Rapid and sustained action based on medication
- Ph Level
- Neutral (as per pharmaceutical standards)
- Strength
- Varies by formulation (generic range: 100 mg, 250 mg, 500 mg, 1000 mg etc.)
- Best Before
- As mentioned on the packaging
- Medicine Type
- Allopathic
- Efficacy
- Highly effective as per pharma standards
- Flavor
- Unflavored or as per requirement
- Purity
- Greater than 98% (active ingredients)
- Chemical Composition
- According to pharma and client specifications
- Ingredients
- As per client requirement, customizable
- Sub Ingredients
- Specific to formulation provided
- Function
- Therapeutic; as per contract manufacturing
- Dosage
- As prescribed by healthcare professional
- Dosage Guidelines
- Follow doctors prescription
- Dosage Form
- Storage Instructions
- Store in a cool, dry place
- Packaging Size
- Customizable (10, 20, 30, 50, 100 tablets/capsules/etc.)
- Packaging Type
- Blister Pack, Bottle, Alu-Alu pack, Strip etc.
- Regulatory Documentation
- Complete support with Dossiers, COPP, stability, and analytical reports
- Customization Options
- Formulation, packaging, branding based on client needs
- Clinical Support
- Product dossiers, stability reports, and regulatory compliance guidance
- Export Capability
- Available; products compliant to international regulations
- Market Segments Served
- Government tenders, retail, hospitals, clinics, and OTC
- Contract Services
- Third party manufacturing, private labelling, product development
- Lead Time
- Typically 4-8 weeks post order confirmation
- Technology Used
- Cutting-edge granulation, coating, encapsulation, and sterile manufacturing units
- Minimum Batch Size
- Varies as per client requirement, typically 5000 units
- Quality Assurance
- Stringent multi-level QA checks, stability and efficacy testing
- Manufacturing Capacity
- High-volume automated plants with dedication to bulk and exclusive batches
- Compliance Certifications
- WHO-GMP, ISO, FSSAI, DCGI approved manufacturing facilities
- Logistics Support
- End-to-end shipment, cold chain management for sensitive products
- Customer Support
- Dedicated account management, technical and regulatory assistance
Third Party Manufacturer For Pharma Trade Information
- Main Export Market(s)
- Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
- Main Domestic Market
- West India
About Third Party Manufacturer For Pharma
Targeted Usage, Competitive Advantage & Guided Application
Our Third Party Manufacturer For Pharma is engineered for diverse applicationsranging from government tenders to hospital supply and retail chains. The key advantage is our client-based customization: choose formulations, dosage forms, and branded designs as per your therapeutic and market needs. With professional guidance, use medicines precisely as prescribed by healthcare professionals to ensure optimal efficacy and safety. Store products in recommended conditions to preserve shelf life and effectiveness.
FOB Port Details, Compliance Certifications & Sample Offerings
Products are delivered through major Indian FOB ports, ensuring global reach. All exports and domestic supplies come with international certificationsWHO-GMP, ISO, FSSAI, and DCGIfor verified quality. Upon purchase order confirmation, we offer flexible sample policies so you can test quality before bulk investment. Our fast and secure delivery networks, allied with comprehensive documentation, guarantee peace of mind and regulatory compliance in every shipment.
FAQs of Third Party Manufacturer For Pharma:
Q: How does the third-party manufacturing process work with your company?
A: Our process begins with your inquiry and product requirement, followed by sample formulation and approval. Once the purchase order is placed, we manufacture in WHO-GMP, ISO, FSSAI, and DCGI-certified facilities. After rigorous quality checks and regulatory documentation, products are packed and shipped as per your specifications.Q: What are the benefits of choosing your pharma manufacturing services?
A: We offer customizable solutions, rapid lead times (48 weeks), compliance with international standards, and robust support for product development, private labelling, and export documentation. Our high-capacity automated plants ensure efficiency, consistency, and competitive pricing.Q: When can clients expect delivery after placing an order?
A: Typically, delivery is completed within 4 to 8 weeks post order confirmation, depending on the product complexity and regulatory requirements. Logistics support, including cold chain management, is also available for sensitive shipments.Q: Where are your manufacturing and export activities based?
A: Our facilities are located in India and adhere to stringent WHO-GMP, ISO, FSSAI, and DCGI standards. We export globally through prominent Indian FOB ports, ensuring reliable access to international markets.Q: What documentation and regulatory support do you provide?
A: We offer complete regulatory assistance, including dossiers, COPP, stability, and analytical reports for global market entry, supported by a dedicated account management and technical support team for smooth compliance.Q: How do I use and store the pharmaceuticals provided?
A: Medications should be taken strictly as prescribed by a qualified healthcare professional. For best results, follow dosage guidelines, and store all products in a cool, dry place away from direct sunlight, as specified on the packaging.
Price:
- 50
- 100
- 200
- 250
- 500
- 1000+
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