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How to Develop a Sustainable Generic Drug Development Strategy

Drug Patent Watch

This article outlines key considerations and strategies for developing a sustainable generic drug development strategy. Pfizer, for example, has been applying green chemistry principles in drug development for over two decades to reduce waste, minimize resource use, and develop energy-efficient manufacturing processes.

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The Benefits of Integrated CDMO Services: Streamlining Drug Development and Manufacturing

Drug Patent Watch

This shift has led to the emergence of integrated contract development and manufacturing organizations (CDMOs), which provide end-to-end support for drug developers. from 2023 to 2030. from 2023 to 2030. Reshaping drug development through CRO/CDMO integration. References Patheon. 2023, August 31).

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Pharma Contract Sales Outlook 2025–2030: Multilingual Teams Drive Global Expansion

The Pharma Data

Billion by 2030: Strategic Insights, Regional Trends, and Technological Shifts Reshaping the Landscape The global pharmaceutical contract sales outsourcing (CSO) market is entering a transformative phase, with its value expected to grow from $17.3 billion by 2030 , reflecting a compound annual growth rate (CAGR) of 6.2%.

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How organoids can redefine pre-clinical research

Drug Target Review

The substantial value of organoids is becoming increasingly recognised by supportive government initiatives developing novel drugs, with a growth rate of 22 percent between 2023 and 2030 and a market size predicted to reach over US $6.5 billion by 2030. Front Genet. 2021;12(November):1–14. Nat Rev Methods Prim [Internet].

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Elevating Employee Experience (EX) in the Age of AI

Perficient: Drug Development

trillion talent shortage projected by 2030. Addressing the Talent Shortage While fears of AI-driven job displacement dominate headlines, the real crisis looming is a $8.5

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Generative AI: Transforming Healthcare Payers from Cost Centers to Value Creators

Perficient: Drug Development

As the healthcare AI segment is poised to reach $187 billion by 2030, organizations must act swiftly to secure a competitive edge or risk being left behind. According to recent insights, 81% of executives expect AI to drive industry-wide efficiency gains of over 25% in the next two years.

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Breaking down barriers across the DMTA cycle

Drug Target Review

Each team supplies valuable insights throughout the design-make-test-analyse (DMTA) cycle to enable the effective design and optimisation of high-calibre drug candidates. Providing specialist and unique insight, CROs can propel a drug discovery process forward.