• FSSAI & AYUSH Approved
  • WHO-GMP
  • ISO 9001:2015
  • PAN India
  • contact@3rdpartypharma.com
  • +91 9990906939
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Third Party Pharmaceutical Manufacturer in India

One WHO-GMP certified facility, every major dosage form. If you’re comparing pharmaceutical manufacturing companies for a product range that spans tablets, capsules, syrups, injectables, and topicals — this is what working with a single manufacturer across your entire portfolio actually looks like.
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WHO-GMP

Certified

ISO 9001:2015

Certified

FSSAI

Approved

AYUSH

Approved

100%

Quality Assurance

10+

Product Categories

500+

Products

100+

Brands

10+

Years Experience

Pharmaceutical Manufacturing Company — Who We Are

Most brands don’t need just one dosage form manufactured. A pharma company launching a cardiac range might need tablets today and an injectable formulation next year. A nutraceutical brand expanding into pharmaceuticals might start with syrups and eventually need capsules. Managing that kind of growth across three or four different manufacturers — each with its own documentation style, its own quality standard, its own account manager — creates friction that most businesses could do without.
We built our operation to solve exactly that problem. As a pharma manufacturing company Delhi brands turn to when their portfolio outgrows a single-format supplier, we run production across seven major dosage form capabilities under one WHO-GMP certified roof — so your product range can grow without your list of manufacturing partners growing alongside it.

Finished Dosage Form Manufacturer — Every Format We Cover

Depth across dosage forms is what separates a genuine finished dosage form manufacturer from a facility that only does one or two formats well. Here’s our full capability range — each links through to a dedicated page with the technical detail for that format.
Tablets
Tablets
Softgel Capsules
Softgel Capsules
Chewable Tablets
Chewable Tablets
HPMC (Veg. Capsules)
HPMC (Veg. Capsules)
Mouth Dissolving Tablets
Mouth Dissolving Tablets
Syrup
Syrup
Powder
Powder
Sachet
Sachet
Effervescent Tablets
Effervescent Tablets
Injectables
Injectables

Our Pharmaceutical Manufacturing Services

Beyond dosage form capability, the actual scope of what we offer as pharmaceutical manufacturing services covers the full journey from formulation to finished, packed product:
  • Formulation development and selection — as a pharmaceutical formulation manufacturer, we work from an existing catalogue formulation or build a custom formula around your specific molecule combination
  • Raw material sourcing and testing — identity and purity verification before any material enters production
  • WHO-GMP certified production — across all seven dosage form capabilities, under one quality system
  • In-house quality control and release testing — batch-level testing appropriate to each dosage form's specific requirements
  • Packaging and labelling compliance — CDSCO, FSSAI, or AYUSH label verification depending on your product category
  • PAN India dispatch and logistics — from a single Delhi NCR facility to your distribution network nationwide
For brands running what amounts to turnkey pharmaceutical manufacturing — where we handle everything from raw material to shipped, branded product — this is the full-service version of what we do. For clients who prefer to manage certain stages themselves (their own packaging design, their own distribution arrangements), the same services are available modularly.

Have a Multi-Product Manufacturing Requirement?

Tell us your product range across dosage forms and we’ll map out what’s ready-to-manufacture and what needs custom development.
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Generic Pharmaceutical Manufacturing vs Branded Generics

This distinction trips up a lot of first-time clients, so it’s worth clarifying directly. Generic pharmaceutical manufacturing refers to producing a formulation using the same active ingredient, dosage, and route of administration as an existing approved product — without a proprietary brand name attached at the manufacturing stage. What happens next is where the paths split.
Aspect Generic Manufacturing Branded Generics
Active Ingredient Same as reference product Same as reference product
Brand Name Sold under generic/salt name Sold under a proprietary brand name
Marketing Approach Price-competitive, often government tenders Built around brand trust and doctor relationships
Who Typically Buys This Distributors, institutional buyers PCD franchise, retail-focused brands
As a branded generics manufacturer serving India’s pharma market, most of our client base falls into the second category — companies building a brand identity around formulations that are chemically identical to what’s already approved and available, differentiated through packaging, pricing, and market positioning rather than the formulation itself.

Why Brands Choose Pharma Manufacturing Outsourcing

Setting up an in-house pharmaceutical manufacturing facility in India typically requires anywhere from one to three years and several crores in capital investment, before a single certified batch is produced. Pharma manufacturing outsourcing — working with an established, certified manufacturer instead — compresses that timeline dramatically and redirects capital toward the parts of the business that actually build market share: distribution, sales infrastructure, and brand development.
This is exactly why so much of the Indian pharma industry — particularly the PCD franchise segment — runs on outsourced manufacturing relationships rather than in-house production. It’s not a compromise; it’s the standard operating model for a large share of the market.

Quality Systems Behind Every Batch

System / Certification What It Governs
WHO-GMP Certification Good Manufacturing Practice compliance across facility design, process control, and documentation
ISO 9001:2015 Quality management system covering consistency of process and continuous improvement
Batch Manufacturing Records Full traceability from raw material lot to finished, dispatched product
In-House QC Laboratory Testing appropriate to each dosage form — physical, chemical, and microbial parameters
Certificate of Analysis Issued with every batch, covering all tested parameters relevant to that product

Why Choose us as your WHO-GMP Certified Pharmaceutical Manufacturer

Seven dosage form capabilities, one quality standard

Whether your range needs tablets, injectables, or topicals, you're working with the same facility, the same documentation system, and the same account relationship throughout.

Genuine multi-dosage manufacturing experience

As a multi-dosage pharmaceutical manufacturer, we're not treating any single format as an afterthought bolted onto a core specialty — each capability is run by teams with format-specific expertise.

Both generic and branded generic production

Whether you're supplying institutional buyers with generic formulations or building a retail brand around branded generics, the manufacturing process and quality standard stay consistent.

Full-service or modular — your choice

Take the complete turnkey service from formulation through to branded dispatch, or manage certain stages yourself. We adapt to how your business actually operates.

Transparent batch documentation, every time

Certificate of Analysis and full batch records accompany every order — the kind of documentation your distributors and regulators expect without having to chase it down.

Delhi NCR positioning works in your favour

Proximity to CDSCO, active state licensing offices, and strong logistics connectivity translate into faster regulatory turnaround and more predictable delivery timelines.

Frequently Asked Questions (FAQs)

Yes — this is actually one of the main advantages of working with a manufacturer offering multiple dosage form capabilities. If your brand needs tablets, syrups, and topicals under the same product line, all three can be manufactured through a single relationship rather than coordinating across separate manufacturers with different documentation standards.
Yes. Whether you need generic pharmaceutical manufacturing for institutional or price-sensitive markets, or branded generics with your own packaging and market positioning, both are available from the same facility under the same quality standard.
Our facility is WHO-GMP certified and ISO 9001:2015 certified, with in-house quality control testing appropriate to each dosage form we manufacture. Certificates are available for review before you commit to a manufacturing agreement.
If you’re a first-time brand wanting to launch a product with packaging and branding support, look at our private label manufacturing service. If you’re a PCD franchise or distributor needing recurring production across therapeutic segments, our third party and contract manufacturing service fits better. If you’re unsure, just tell us what you’re trying to build — we’ll point you to the right arrangement rather than let you guess.

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