Vix Pharma International

Third Party Pharma Manufacturing Company

Vix Pharma International is a WHO-GMP and ISO 9001 certified Nutraceuticals contract manufacturer based in Delhi NCR. With a comprehensive range of over 500 formulations across all major therapeutic segments, Vix Pharma delivers quality medicines — custom branded, regulatory-compliant, and dispatched PAN India.
Company at a Glance
500+

Products in Portfolio

15+

Years of Experience

WHO-GMP

Certified Facility

ISO 9001

Certified Facility

About Vix Pharma International

Vix Pharma International is a Delhi NCR-based WHO-GMP certified third party pharmaceutical manufacturing company that has built a strong reputation in India’s contract pharma manufacturing sector. The company operates a state-of-the-art, fully-compliant manufacturing facility where quality is not a checkpoint — it is embedded into every stage of the production process, from raw material sourcing to final dispatch.
Over the years, Vix Pharma International has established itself as a dependable name for pharma brands, PCD franchise operators, and healthcare companies across North India and beyond. The company’s manufacturing setup covers a wide spectrum of dosage forms — tablets, hard and soft gelatin capsules, liquid orals, dry syrups, ointments, creams, injectables, eye drops, and nutraceutical preparations — all manufactured under rigorous in-house quality control protocols.
What sets Vix Pharma apart in a crowded marketplace is a genuine commitment to transparency. Every batch comes with a full Certificate of Analysis. Every raw material entering the production floor is tested before use. Every client — whether a startup launching their first brand or an established distributor expanding their portfolio — receives the same standard of manufacturing excellence. Vix Pharma International’s manufacturing facility is located in Delhi NCR’s pharmaceutical industrial zone, offering strategic advantages for logistics, regulatory interactions, and talent access. The company serves clients across all 28 Indian states and holds the capability to fulfill international export orders for regulated and semi-regulated markets.

Key Business Highlights

200+

Approved Formulations in Product Portfolio

WHO-GMP

Internationally Recognized Quality Certification

Delhi NCR

Manufacturing Base — North India's Pharma Hub

B2B

Third Party & Contract Manufacturing

In-House

Dedicated Quality Control Laboratory

Custom

Private Label & Custom Packaging Available

PAN India

Delivery Across All 28 States & UTs

Export

International Export Capability — Middle East & Africa

Services Offered by Vix Pharma International

Third Party Pharma Manufacturing

Vix Pharma International's core offering — your brand, your formulation specs, manufactured in a WHO-GMP certified facility with full batch documentation and COA per dispatch.

Contract Manufacturing
(CMO)

Long-term contract manufacturing arrangements for pharma companies needing consistent, high-volume production with guaranteed capacity allocation and dedicated production lines.

Private Label / OEM Manufacturing

Complete private label manufacturing service — your brand name, your packaging design, your label content. Vix Pharma handles everything from artwork verification to dispatch.

Custom Formulation
& R&D

In-house R&D capability for novel drug combinations, specific strengths, modified release formulations, and combination products not available off-the-shelf.

Product Range — Vix Pharma International

Specialised Focus Areas

Gynecology

Women's health formulations across all life stages — from prenatal supplements to menopause support. Developed with precision and backed by stringent quality checks.

Infertility Support

In-house R&D capability for novel drug combinations, specific strengths, modified release formulations, and combination products not available off-the-shelf.

Orthopedics

Joint mobility, bone strength, and pain management formulations. Oral tablets and supplements designed for an active, pain-free lifestyle.

Gym & Sports Nutrition

A comprehensive nutraceutical range for fitness brands — Creatine, Glutamine, Protein blends, Immunity boosters, and Pre-workout formulations.

Nutraceuticals

Vitamins, minerals, antioxidants, herbal extracts, and functional food supplements — all manufactured under FSSAI and WHO-GMP certified conditions.

Ayurvedic Preparations

Classical and proprietary Ayurvedic formulations — oils, juices, churnas, tablets, and herbal preparations under AYUSH-compliant manufacturing protocols.

Step-by-Step Third Party Pharma Manufacturing Process

A lot of first-time clients come to us with one question: “Exactly how does this work?” Fair enough. The pharmaceutical contract manufacturing process might sound complicated from the outside, but in practice — with the right partner — it’s quite structured. Here’s how it typically unfolds:

Initial Consultation & Product Selection

You share your target therapeutic segment and required products — or browse our existing formulation catalogue. Our team discusses MOQ, pricing, lead times, and regulatory scope. If you need a custom formulation, this is where R&D discussions begin too.

Document Submission & Agreement Signing

You submit your Drug License, GST certificate, company registration documents, and brand details. A formal manufacturing agreement — covering product specs, pricing, payment terms, delivery schedules, and IP clauses — is signed. An NDA protects your formulation confidentiality.

Artwork & Packaging Approval

You submit your packaging design, logo, label content. We check it against CDSCO labelling guidelines — mandatory information, font size, Rx symbol, batch/expiry placement. Final artwork is approved before production starts. Delays here = delays in dispatch, so have artwork ready in advance.

Raw Material Procurement & Incoming Quality Check

Only pharmacopoeial grade, DCGI-approved raw materials from certified vendors are used. Every incoming batch goes through identity testing, assay, and purity checks before it enters the production line. This is a step that separates serious manufacturers from fly-by-night operators.

GMP Manufacturing & In-Process Quality Control

Production happens in our WHO-GMP certified facility under the supervision of qualified pharmacists. In-process quality checks — weight variation, hardness, disintegration, pH, viscosity (for syrups) — happen at every critical stage. A full Batch Manufacturing Record (BMR) is maintained for every production run.

Finished Goods Testing & QC Release

The finished product undergoes complete quality analysis — assay, dissolution, uniformity of dosage, microbial limits, stability testing. Nothing leaves the facility without QC clearance. A Certificate of Analysis (COA) is issued for every released batch — you receive this with every shipment.

Packaging, Dispatch & PAN India Delivery

Products are packed in your custom branded packaging — strips, bottles, tubes, vials — and dispatched to your warehouse or directly to your distributors. Cold chain logistics available for injectables and temperature-sensitive products. PAN India delivery with full tracking.

Why Partner with Vix Pharma International?

WHO-GMP Certified — Not Just Claimed

Vix Pharma International holds valid, inspected WHO-GMP certification for its manufacturing facility. Clients can request site visits and certificate verification before committing — that level of transparency is how trust is built.

500+ Ready-to-Manufacture Formulations

With an approved portfolio spanning all major therapeutic segments, Vix Pharma gives you the ability to build a comprehensive product range quickly — without waiting months for new product approvals.

Delhi NCR Location — Strategic Advantage

Manufacturing in Delhi NCR means faster access to CDSCO, North India's largest distribution network, and seamless logistics connectivity to every corner of the country — and to export markets via IGI Airport.

Per-Batch COA — Zero Compromise on Documentation

Every dispatched shipment comes with a signed Certificate of Analysis covering all relevant quality parameters. This documentation supports doctor and pharmacist trust in your brand — and protects you legally.

Flexible MOQ — Accessible for New Brands

Vix Pharma International's manufacturing structure accommodates new entrants with lower minimum order quantities for initial batches — so you can validate quality and market response before scaling up.

Custom Formulation R&D Available

When an off-the-shelf formulation doesn't fit your brand vision, the in-house R&D team at Vix Pharma develops custom formulations — novel combinations, specific strengths, modified release formats.

Dedicated Account Management

You get a single point of contact who knows your brand, your product list, and your delivery requirements. No being transferred across departments — direct, responsive communication from enquiry to delivery.

Complete Private Label & Branding Support

Packaging design guidance, CDSCO artwork compliance verification, regulatory labelling review — Vix Pharma International makes the private label process straightforward for both new and experienced brand owners.

Ready to Launch Your Pharma Brand in Delhi NCR?

Talk to our team today — WHO-GMP certified facility, 500+ products, flexible MOQ, and PAN India delivery. Free consultation, no obligations.

Frequently Asked Questions (FAQs)

For domestic Indian clients, you need a valid Drug License (Form 20 & 21), GST registration certificate, and your company registration documents. For international buyers, import/export documentation and the relevant licenses from your country are required. Our team helps guide you through the documentation process — especially for first-time clients.
New product orders — where artwork and formulation need to be finalized first — typically take 20–25 working days after all documentation is complete. For repeat or running products already in the system, the turnaround is faster: 15–20 working days. These timelines are consistently maintained across both domestic and export orders.
Vix Pharma International holds six active certifications: WHO-GMP, ISO, FSSAI, HACCP, GMP, and FDA compliance. These certifications cover both pharmaceutical and nutraceutical/food supplement manufacturing, making Vix Pharma eligible for domestic and international (export) production orders.
The minimum order quantity starts from 3,000 bottles/units for standard products. MOQ can vary depending on the specific dosage form and formulation. For custom or specialty products — like Ashwagandha supplements or Effervescent Tablets — contact Vix Pharma directly for an exact MOQ and pricing quote.
Yes — private label manufacturing is one of Vix Pharma’s core services. This includes custom formulation development, branded packaging design support, CDSCO label compliance verification, and dispatch under your brand name. Both new brands launching their first product and established companies expanding their portfolio are served under this model.
Vix Pharma International’s core specialisation is Nutraceuticals, Dietary Supplements, and Ayurvedic preparations. Within pharma, the company manufactures across multiple dosage forms including tablets (regular, chewable, effervescent, mouth-dissolving), capsules (gelatin and HPMC), soft gels, syrups, cough syrups, sachets, powders, injectables, Ayurvedic oils, herbal juices, and topical preparations.
Yes. The in-house R&D team at Vix Pharma International handles custom formulation development — novel drug or supplement combinations, specific strengths, modified release formats, and new delivery systems for both pharma and nutraceutical products. Custom development timelines vary but are discussed transparently at the consultation stage.

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