NEXLIFE BIOSCIENCE PRIVATE LIMITED
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Pharmaceutical Third Party Manufacturing Service
Pharmaceutical Third Party Manufacturing Service

Pharmaceutical Third Party Manufacturing Service

MOQ : 1 Unit

Pharmaceutical Third Party Manufacturing Service Specification

  • Indication
  • As per prescribed use of manufactured products
  • Origin of Medicine
  • India
  • Dosage Form
  • Oral, Injectable, Topical, Liquid
  • Salt Composition
  • Available according to client specification
  • Pacakaging (Quantity Per Box)
  • Customized as per client need
  • Drug Type
  • Allopathic
  • Ingredients
  • Custom formulations as per clients requirements
  • Physical Form
  • Tablet, Capsule, Syrup, Injection, Ointment, Powder, Liquid
  • Function
  • Manufacturing of pharmaceutical formulations under third party protocols
  • Recommended For
  • Pharmaceutical Companies seeking manufacturing support
  • Dosage
  • As per prescribed medical standards and client specifications
  • Dosage Guidelines
  • As indicated by medical professional or product specification
  • Suitable For
  • Adults and children as per product
  • Quantity
  • Bulk/Contract-based quantity
  • Storage Instructions
  • Store in a cool, dry place away from direct sunlight
  • Documentation Support
  • Full regulatory documentation provided
  • Product Certification
  • ISO, GMP, WHO compliance as per product
  • Customization
  • Label, packaging, formulation as per client
  • Customer Support
  • Dedicated assistance for project coordination
  • Service Type
  • Third Party/Contract Manufacturing
  • Manufacturing Capacity
  • High capacity for bulk production
  • Quality Assurance
  • Stringent quality checks and laboratory testing
  • Minimum Order Quantity
  • Negotiable, as per product category
  • Shelf Life
  • As per product specification (generally 12-36 months)
 
 

About Pharmaceutical Third Party Manufacturing Service



Experience remarkable Pharmaceutical Third Party Manufacturing Service in India, designed exclusively for pharmaceutical companies pursuing opulent product reliability. Take advantage of Advance Purchase opportunities, ask about our limited-time Price Cut promotions, and leverage our industry-best service for bulk production needs. Fully ISO, GMP, and WHO-compliant, our solutions provide stringent quality assurance and laboratory testing across tablets, capsules, syrups, injections, ointments, powders, or liquids. Benefit from fully customizable label, packaging, and formulation with robust documentation for regulatory compliance. Our dedicated customer support and high-capacity manufacturing deliver peace of mind and lasting value, with negotiable order quantities and bespoke product certification.

Versatile Pharmaceutical Manufacturing for Global Markets

Our Pharmaceutical Third Party Manufacturing Service is ideal for pharmaceutical companies seeking reliable, contract-based manufacturing solutions that suit both adult and pediatric requirements. Usable in various medical sectors-including hospitals, clinics, and retail pharmacies-our plant supports advanced manufacturing for tablets, capsules, syrups, and more. With impeccable control over quality, formulation, and packaging, we're equipped to support your brand's presence worldwide. Each partnership ensures custom solutions tailored to your application and distribution needs.


Export-Ready Services with Secure Valuation and Shipping

We facilitate seamless export market access via reliable FOB Ports across major Indian hubs. All orders are meticulously packaged according to client specifications, prioritizing protection and compliance for domestic and global distribution. Using advanced secure shipping practices, we ensure your products are delivered intact and on time. Valuation for contracts and sample policies is transparent and negotiable to help you make informed, risk-free decisions as you expand your market reach.


FAQ's of Pharmaceutical Third Party Manufacturing Service:


Q: How can I benefit from your third party manufacturing service for pharmaceuticals?

A: Our service enables pharmaceutical companies to outsource manufacturing with full compliance to ISO, GMP, and WHO standards, customized formulations, branded packaging, and comprehensive regulatory support while saving on operational overhead and ensuring rapid market entry.

Q: What is the process for starting a contract manufacturing project?

A: Simply reach out with your requirements. We assess the formula and product, align compliance standards, finalize order details including price, packaging, and documentation, and begin manufacturing once all terms are confirmed and samples are approved by you.

Q: Where are your manufacturing facilities located?

A: Our advanced manufacturing plants are based in India, equipped with modern technology and certifications required for high-capacity, compliant pharmaceutical production for global and domestic markets.

Q: When can I expect delivery and what are the shipping terms?

A: Delivery timelines depend on formulation complexity and order quantity, but we prioritize efficient production and secure shipment using established FOB ports in India to ensure timely international and domestic delivery.

Q: How do you ensure the quality and safety of products?

A: Stringent laboratory testing and quality checks are conducted at every stage of the process, ensuring each product batch meets the highest standards for efficacy, safety, and compliance according to certifying bodies and client requirements.

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