Emerging Market Outsourcing Report - Q2 2025

This expert outsourcing report is a comprehensive look at the pharmaceutical manufacturing landscape for emerging markets in Q2 2025, including analysis of news and trends affecting contract manufacturing organizations (CMOs) and the identification of recent contract service agreements, mergers, acquisitions, and financing among CMOs. It is a critical source for strategic planning efforts and will improve understanding of crucial components of the pharmaceutical value chain that will provide insights into API (biologics and chemical) as well as dose manufacturing and packaging (clinical and commercial) for countries in emerging markets.

Scope

This report gives an important monthly update on the pharmaceutical outsourcing industry, based on analysis from GlobalData's experts and our databases covering deals, companies, drugs, financials, news, clinical trials, and more. This report is required reading for -

• CMO executives and strategic decision-makers: to improve understanding of the CMO industry and provide a critical input for strategic planning efforts.
• Sourcing and procurement executives in bio/pharmaceutical companies: to improve understanding of crucial components of the supply base that will provide insights for supplier selection and management.
• Investors, advisors, and consultants: they can gain a deeper understanding of the CMO market and important insights for identifying potential investment targets.

Reasons to Buy

This report will enable the user to answer the following questions -

• What are the latest trends in contract service agreements within the emerging markets of the pharmaceutical industry such as India, China, the Middle East, South America, and Eastern Europe?
• What mergers and acquisitions have occurred in the pharmaceutical sector during Q2 2025, and what do they signify for the industry?
• How are global supply chains for active pharmaceutical ingredients (APIs) being affected by regulatory changes and inspections?
• What are the key challenges and opportunities for contract research, development, and manufacturing organizations (CRDMOs)?
• What are the outcomes of FDA inspections and compliance issues for pharmaceutical manufacturers?