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EMA proposes streamlined approach for biosimilar development

European Pharmaceutical Review

The European Medicines Agency (EMA) has published a new draft reflection paper , which discusses reducing the quantity of clinical data needed for development and regulatory approval of biosimilars. This is part of the agencys work to improve the development and assessment of biosimilar medicines, while maintaining EU safety standards.

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Real estate continues to fuel growth of Indian life sciences; provide platform for global ascent in 2025

Express Pharma

At the same time, Indias growing focus on tapping the $36 billion global biosimilars market highlights the need for real estate infrastructure that can support advanced manufacturing capabilities. This tech-driven evolution has been mirrored in the demand for state-of-the-art research and development (R&D) facilities and production hubs.

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CPHI & PMEC India expo to be held from Nov 26-28, 2024

Express Pharma

India’s pharma industry is on an impressive growth trajectory, expected to reach $65 billion by 2024 and to double to $130 billion by 2030. Renowned as a comprehensive, one-stop destination for innovative, cost-effective solutions, the expo will be showcasing the pharmaceutical industry’s modernisation, innovation, and sustainability.

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Sudarshan Jain highlights Indian pharma’s path to $130 billion by 2030

Express Pharma

The patent expiries of blockbuster biologics by 2025 present a significant growth avenue in the global biosimilars market. Indian pharma market is expected to move up to USD 120-130 Billion by 2030 from current size of USD 58 Billion.

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17th edition of CPHI & PMEC India inaugurated at India Expo Centre, Noida

Express Pharma

With the Indian pharma market projected to grow to $ 130 billion by 2030 and $ 450 billion by 2047, the event highlighted the industry’s vital role in shaping global healthcare. Projections indicate exports will soar to $130 billion by 2030 and $450 billion by 2047. With exports nearing $27.84

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Dr Reddy’s completes Phase I study of DRL_TC, a tocilizumab biosimilar candidate

Express Pharma

Dr Reddy’s Laboratories announced that its tocilizumab biosimilar candidate, DRL_TC, successfully met its primary and secondary endpoints in a Phase I study. Dr Reddy’s is developing the proposed tocilizumab biosimilar as both intravenous and subcutaneous formulations.” billion patients by 2030.”

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Basics of Biosimilars

Integra X Files

Drugs vs. Biologics: What’s the Difference If you ask a layperson about biosimilars, you are likely to hear comparisons to generic drugs, and that would not be completely wrong. Biosimilar products are not drugs and they are not generic, in the sense that they’re not identical to the reference product.