
2026 Global Biosimilars Market Midyear Review
Midyear assessment of the global biosimilar market, covering regulatory developments, product approvals, and dealmaking in the US and Europe during the first half of 2026.
Our team of scientists, strategists, economists, clinicians, and biostatisticians stay on the cutting edge of the evolving landscape. We collect their insights and the latest thinking and invite you to explore these resources.
Our team of scientists, strategists, economists, clinicians, and biostatisticians stay on the cutting edge of the evolving landscape. We collect their insights and the latest thinking and invite you to explore these resources.
Access a midyear assessment of the global biosimilar market, covering regulatory developments, product approvals, and dealmaking in the US and Europe during the first half of 2026.

Midyear assessment of the global biosimilar market, covering regulatory developments, product approvals, and dealmaking in the US and Europe during the first half of 2026.

Discover biologics CDMO M&A activity for 2026 with this one pager of insights into transaction volume, geographic distribution, capabilities, and modalities.

Learn about the H1 2026 M&A trends in the medtech CDMO market including deal activity, geographic distribution of transactions, and target end-markets.
Discover how we help our clients solve complex challenges. Explore our collection of case studies to learn more about our approach.

Learn how a targeted recruitment campaign helped enroll six patients in a myasthenia gravis clinical trial in just one quarter, accelerating recruitment.

Discover how an infection prevention company defined a successful US market entry strategy amid regulatory uncertainty for novel wound care disinfectant products.

Discover how a biotech company executed a complex Phase I trial with Alira Health, ensuring seamless coordination of manufacturing, logistics, and sites.
Discover expert interviews featuring thought leadership and practical insights from Alira Health specialists.

Explore how registries in rare disease trial recruitment connect sponsors with patient communities to improve identification and enrollment.

Learn what clinical trial excellence means in complex product development and how biotech leaders can manage new complexity, risk, and executional pressure.

Medtech success requires more than approval. Discover how aligning evidence, patient needs, and market access drives adoption.
Read our articles that provide insight to those innovating and developing in multiple healthcare markets, including pharma, medtech and more.

Discover how patient preference studies use qualitative and quantitative methods to generate decision-Grade Evidence across development and commercialization.

Discover FDA programs in 2026 that foster rare disease drug development, offering guidance, funding, and regulatory support for innovators.

Discover how a strategically planned clinical evidence generation strategy can support global device approval, maximize evidence value, and prepare for international expansion.
Listen to the latest insights from Alira Health experts featured in webinars. Just hit play!

Watch the webinar to get practical insights on cross-border rare disease clinical trials and explore patient-centric strategies that support sponsor execution and patient access.

Educational webinar series about Value-Based Contracting by payers and academic experts and covering VBC fundamentals to success assessment.

This webinar explores how MFN pricing may impact US drug prices, access in Europe, launch strategies, and biotech investment.