01.09.26 -- Trading Places: 2025 Intensified CDMOs Recruiting Sponsor Talent

This event offers short, interactive digital presentations from leading CDMOs showcasing their capabilities, facilities, and available capacity for biopharma development and fill-finish manufacturing. Attendees can explore sterile filling, lyophilization, and packaging technologies, and ask questions live. Open to pharma and biotech professionals, industry consultants, investment firms, and CDMO sponsors seeking manufacturing solutions. Click here to learn more.

Atropisomers are key to modern small molecule drug development. Learn how advanced manufacturing strategies enable the isolation and scalable production of the most effective single isomer.

Discover how continuous manufacturing, AI-driven digital twins, and advanced tooling materials are transforming tablet compression to boost quality and cut operational costs in pharmaceutical production.

Achieving regulatory compliance confidence is paramount for safety and competitive advantage. Adherence to standards and risk mitigation are essential to avoid delays and detrimental outcomes.

A forthcoming ISPE guide uses case studies to aid in the design of plug-and-play process skids with implications for every step in the manufacturing process continuum.

Targeted Protein Degraders are a revolutionary drug class with challenges in bioavailability and formulation complexity. Strategic CDMO partnerships are key to successful, scalable development.

See key strategies for seamless pharmaceutical technology transfers that accelerate time to market, ensure product quality, and meet regulatory standards across the drug lifecycle.

Accelerate the development of ADCs with capabilities spanning clinical to commercial production, including OEB 5 handling, state-of-the-art fill/finish, and future expanded conjugation services.

Digital services on a scale that is unique in the industry, including visual support with augmented reality, remote diagnosis via QR code, and visual spare parts search.

Streamline validation and quality management with a ready-to-use, web-based platform featuring pre-designed process and templates, which eliminates start-up delays and ongoing maintenance.