Resources

Explore our Resources

Access a curated collection of materials designed to provide insights into our capabilities and expertise across the drug development and manufacturing lifecycle.

Whitepaper

Beyond the Molecule: Human Factors Engineering as the Competitive Edge in Drug-Device Combination Products

The molecule isn’t the differentiator anymore. The device is. What this whitepaper covers: How an integrated CDMO turns device usability into commercial advantage for self-administered drug-device combination products. Whitepaper Abstract: For a…

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Industry Perspective

Cyber Risk is now a financial risk: Why pharma boards can’t look away

Anurag Bhagania, CFO, OneSource Specialty Pharma Published on ET Edge Insights Source: Cyber Risk is now a financial risk: Why pharma boards can’t look away – ET Edge Insights Cyber risk is…

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Whitepaper

Lyophilization by Design: Engineering Stability, Speed, and Scale into the Next Generation of Parenteral Products

What this whitepaper covers: Why lyophilization has become a defining constraint in modern biologics development — and how a QbD-led, integrated approach transforms cycle design into a scalable, regulatory-ready system. Whitepaper Abstract:…

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Industry Perspective

The quiet revolution in how we take our medicine

The quiet revolution in how we take our medicine Ravi Kumar, Global Head of Injectables & Corporate Strategy, Portfolio and SPO Published on Money Control, 05 Jun 2026 Three out of four…

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Whitepaper

Bioavailability by Design: Lipid Softgel Technology as a Commercial Rescue Path for Poorly Soluble, Low-Bioavailability Molecules

Solubility is broken. The pipeline proves it. What this whitepaper covers: Why solubility failure is the defining challenge of modern oral drug development — and how self-emulsifying softgel technology (SEDDS/SMEDDS/SNEDDS) unlocks bioavailability…

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Whitepaper

Driving the Shift to Subcutaneous Biologics

The subcutaneous shift has already happened. Is your pipeline ready? In 2000–2004, 25% of FDA biologic approvals were device-based. By 2023-2025, 74% were. OneSource delivers the complete subcutaneous (SC) development stack –…

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On-Demand Webinar

Accelerating GLP-1 Peptides to Market Through Integrated Formulation & Analytical Development

GLP-1 peptide therapeutics are rapidly reshaping the treatment landscape for diabetes and obesity, increasing the need for robust formulation development and comprehensive analytical characterization strategies that enable safe, scalable, and market-ready drug…

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Industry Perspective

Supply chain resilience is not an insurance cost, but value protection

Supply chain resilience is not an insurance cost, but value protection Anurag Bhagania, Chief Financial Officer Published on BW CFO World, 14 Apr2026 For a long time, the ‘ideal’ supply chain was…

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Industry Perspective

CDMOs as innovation partners in R&D

CDMOs as innovation partners in R&D Prateek Gupta, SVP & head, Technical Development Published on Hindustan Times, 22 Mar 2026 Pharma research and development (R&D) is moving faster and getting harder at…

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