About us

Your trusted end-to-end CDMO partner

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Who we are 

We’re India’s first specialty pharma pure-play CDMO.

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. So, while others might stand in your way, 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, a Strides Pharma initiative, has a strong legacy 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, all under one roof. So you don’t have to.

Customer-first. Always.

We’re reliable, transparent and fast. We will do whatever it takes to solve your challenges. Our dedicated tech transfer and project management teams are agile, efficient and will work with you in full transparency.

Unique breadth of technical expertise

Our technical expertise is second to none. We’re experts in every discipline we work in across multiple drug product formats and drug substance technologies, with proven track record and legacy in formulation, drug-devices and oral technologies.

Robust quality and compliance standards

Quality, compliance and confidentiality are a non-negotiable for us – in everything we do. From our regulatory approved facilities to robust Quality Management Systems (QMS) and track record of 18 successful inspections in the last 24 months.

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

Our responsibility

Environmental, Social and Governance (ESG) standards

We put the planet and its people first. At our manufacturing sites, 78% of our energy needs are already met by renewable sources like solar and wind power. But we’re not stopping there. We have targets in place to achieve: 

  • 90% renewable energy by 2026 
  • 100% renewable energy by 2030 

To further reduce our environmental footprint, we’re using LPG in our boiler systems to lower carbon emissions, and we’ve adopted water recycling and desilication processes to maximize water recovery and minimize raw water usage. 

But sustainability isn’t just about the environment. We’re deeply invested in uplifting the communities where we operate, such as in Doddaballapur, India. From installing water plants to improving local schools, we take action to support and develop these communities.  It’s not just our Corporate Social Responsibility (CSR) – it’s our commitment to creating lasting positive impact. 

Discover a partnership where you and your ideas come first

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