VO Pharma

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Your Third-Party Manufacturing Partner for Worldwide Markets

We provide end-to-end third-party manufacturing services for worldwide distribution. Our advanced facilities and experienced team ensure every product meets international quality standards. We help you scale your pharmaceutical business with confidence.

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Our Third-Party Manufacturing Services

VO Pharma offers a broad range of products through third-party manufacturing services, serving the growing needs of pharmaceutical brands. We manufacture everything from solid dosage forms to advanced sterile preparations, covering every stage of production with precision and consistency.

We specialize in injectables and sterile manufacturing, using dedicated infrastructure and rigorous quality protocols. This enables us to deliver products that meet the highest international safety and regulatory standards.

OUR ANNUAL CAPACITY

3060

MILLION

TABLETS

 149

MILLION

CAPSULES

330

MILLION

DRY SYRUP

180

MILLION

DRY POWDER INJECTION
 

3470

MILLION

DRY GRANULES
36.7

MILLION

OINTMENTS & CREAMS

1.1

MILLION

SACHETS

14.4

MILLION

SOFTGEL CAPSULES
 

Our Product Range

With expertise across multiple dosage forms, we help brands develop a varied and competitive product portfolio.

Our Manufacturing Licenses

We are licensed to produce a broad range of pharmaceutical products, specializing in key therapeutic areas and advanced dosage forms. Our facilities follow strict standards to ensure consistent quality across all products we manufacture.

Sustained Release Tablets

Sustained Release Tablets

Chewable Tablets

Chewable Tablets

Film-Coated Tablets

Film-Coated Tablets

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Ready-to-compress granules for tablets

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Ready-to-fill powders for oral suspensions and capsules

End-to-End Pharmaceutical Manufacturing Services

We provide complete contract manufacturing services, delivering medicines with uncompromising quality and full regulatory compliance.

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Certified Manufacturing Facility
Our WHO-GMP and GLP-certified plant ensures safe and compliant production. We maintain separate sections for Beta-Lactam and Non-Beta-Lactam products to uphold best practices.
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Client Collaboration

We begin by understanding the client’s requirements, including product specifications, formulation, quantity, quality standards, and timelines.
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Formulation & Raw Material Management

Clients provide formulations and APIs, while we source excipients and other raw materials from approved suppliers. All inputs undergo strict quality checks to ensure compliance.
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Production & Quality Assurance

Our manufacturing processes, blending, granulation, tablet pressing, encapsulation, or other techniques, are executed under stringent quality control to meet compliance standards.
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Packaging & Documentation

Products are packaged and labeled according to client specifications and regulatory norms. Complete documentation is maintained for traceability and compliance.
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Delivery & Regulatory Support

Finished products are delivered on time to the client’s designated location. We also assist with regulatory filings, such as new drug or abbreviated applications, where required.
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Start Your Pharmaceutical Manufacturing Journey with Us

Partner with a team that converts your formulations into high-quality products ready for global markets. From regulatory guidance to on-time delivery, we handle the complexities so you can focus on growing your business.

Take the next step: share your product requirements, and we’ll create a manufacturing plan just for you.

Contact Us
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We’re Ready When You Are

We provide full-service pharmaceutical manufacturing with global-quality standards, regulatory compliance, and reliable delivery. Let us help bring your formulations to market, whether you serve local customers or expand internationally.

Get in touch today and start delivering your innovations to life.

Connect With Our Experts

Take the advice of our experts and make the best decisions.

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