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Third Party Manufacturing

Third Party Manufacturing

Chemo Biologicals Limited is a trusted name in the pharmaceutical industry, offering excellent opportunities for individuals and businesses through our PCD Pharma Franchise model. With years of expertise and a strong reputation, we provide a reliable platform for entrepreneurs who wish to establish their presence in the pharma sector with minimal investment and maximum returns. Our PCD Pharma Franchise program is designed to give you exclusive monopoly rights, ensuring that you face minimal competition in your chosen territory. We provide a wide range of DCGI-approved products, including tablets, capsules, syrups, injections, ointments, and more, covering multiple therapeutic segments such as antibiotics, cardiac, diabetic, gynecology, dermatology, gastro, respiratory, and oncology.

Another major advantage of third party manufacturing is flexibility. Companies can scale production as per market demand without worrying about capacity or resources. Moreover, reputed manufacturers follow strict quality assurance processes, GMP & WHO guidelines, and maintain advanced packaging standards to meet both domestic and international requirements. For businesses looking to establish their brand in the competitive pharmaceutical sector, third party manufacturing offers a reliable pathway. It not only saves time and cost but also helps in building a strong market presence with quality-driven products. With a trustworthy manufacturing partner, companies can achieve growth, expand their reach, and create a lasting impact in the healthcare industry.

About Chemo Biologicals

Third Party Manufacturing Benefits

Comprehensive advantages of partnering with Chemo Biologicals

Cost-Effective Production

Saves investment on infrastructure, machinery, and workforce by outsourcing manufacturing.

Exclusive
Focus on Core Business

Companies can concentrate on marketing, branding, and sales while experts handle production.

Affordable
High-Quality Standards

Products are manufactured in WHO-GMP/ISO-certified units with strict quality checks.

Certified
Wide Product Range

Access to diverse formulations without maintaining in-house R&D and manufacturing.

Scalability & Flexibility

Easy to increase or modify production volumes as per market demand.

Faster Market Entry

Quick product launches without delays in setting up a manufacturing unit.

How to Start Third Party Manufacturing

Simple step-by-step process to become our franchise partner

1
Choose Manufacturer

Select a reliable and experienced pharma manufacturer who offers quality products, certifications, and timely delivery to ensure smooth third-party manufacturing for your business.

2
Select Products

Choose the right formulations from the manufacturer’s product list that match your business needs, market demand, and customer preferences for better growth.

3
Prepare Documents

Submit required licenses, GST, and legal papers to comply with pharma regulations and ensure smooth third-party manufacturing approval.

4
Approve Packaging

Finalize packaging design and labeling that meets regulatory norms, ensures product safety, and enhances brand identity with clear details.

5
Check Quality

Ensure every pharma product meets strict quality standards by verifying certifications, conducting inspections, and following regulator.

6
Sign Agreement

Finalize the contract to begin business with assurance of trust, quality, and timely supply.

Territory Availability

Explore available franchise opportunities across India

North India

Delhi, Punjab, Haryana, Rajasthan, UP, Uttarakhand, HP, J&K

15+ Districts Available
South India

Karnataka, Tamil Nadu, Andhra Pradesh, Kerala, Telangana

12+ Districts Available
East India

West Bengal, Odisha, Bihar, Jharkhand, Assam, Tripura

10+ Districts Available
West India

Maharashtra, Gujarat, Madhya Pradesh, Goa, Chhattisgarh

18+ Districts Available

Ready to Start Your PCD Pharma Business?

Join hundreds of successful partners across India. Get monopoly rights for your territory today!

Free Consultation
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24/7 Support

Frequently Asked Questions

Get answers to common questions about Third Party Pharma Manufacturing

Third Party Manufacturing is when a pharma company outsources the production of medicines to a certified manufacturer and sells them under its own brand name.

Required documents include Drug License, GST Registration, Company Profile, PAN Card, and Packaging Details. Our team provides full guidance during documentation.

The MOQ depends on the product type, usually starting from 500 to 1000 units. However, small batch manufacturing is also available for new businesses.

Investment depends on the number of products and packaging requirements. Small orders need less capital, making it affordable for startups.

On average, Third Party Manufacturing takes 30–45 days after finalizing the composition, packaging design, and necessary approvals.

It reduces costs, saves time, ensures high-quality standards, and allows pharma companies to focus on marketing and distribution while leaving production to experts.