About us

Your trusted end-to-end CDMO partner

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Who we are 

We are OneSource. The multimodal specialty pharma CDMO with end-to-end capabilities across tech platforms and therapeutic modalities.

With three decades of experience in specialized drug development and manufacturing, we are able to consistently deliver comprehensive solutions efficiently and effectively across various technology platforms and therapeutic modalities.

Our team of over 1,200 professionals, including more than 200 techno-commercial experts has one goal – to work closely with our partners and make their vision come to life.

We’re here to change the way you think about CDMOs. We deliver your ambitions with agility and flexibility. Why? Because your success is our success.

So here we are, the type of CDMO you didn’t know could possibly exist.

What we do

Explore our capabilities

Capabilities

Our journey  

OneSource has a strong proven track record of manufacturing excellence in the pharmaceutical and biotechnology industries.

Our values

Integrity

We adhere to ethical practices and maintain transparency in our conduct, fostering a culture of trust and integrity in the organisation.

Competency

We develop and effectively apply our knowledge, abilities and skills to successfully and consistently deliver desired outcomes.

Efficiency

We are agile and collaborative to deliver quicker and better results.

Not just another pharmaceutical CDMO

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End-to-end services across multiple modalities

From early stage development to commercialization and lifecycle management, we can advise and deliver on all your unique requirements, taking care of the complexities so you don’t have to.

Customer-first Always

We are reliable, transparent and fast. With our collaborative and adaptable approach, you can count on us to ensure your project’s success at every stage.

Unique breadth of technical expertise

Our industry-leading expertise supports you from concept to market, including formulation and development, commercialization and life cycle management. Our team provides specialized assistance in drug device development, regulatory support and procurement.

Robust quality and compliance standards

From our regulatory approved facilities to robust Quality Management Systems (QMS) and track record of 138 successful audits across our sites, we ensure quality, compliance and confidentiality at every stage, so you can launch with confidence.

State-of-the-art facilities: A blueprint for success

When it comes to our facilities, there is no room for compromise. That’s why our cutting-edge development and manufacturing sites are equipped with the latest technology and highest standards. Approved by various regulatory bodies, including the FDA, MHRA, ANVISA, TGA, WHO and MCC, our facilities speak for our commitment to excellence.

We currently operate five state-of-the-art facilities in Bengaluru, India, with plans for future expansion coming soon.

Leadership team

Advisory team

Discover a partnership where you and your ideas come first

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