01.29.26 -- Mind The Potent Compounds When Retrofitting Facilities For ADCs

Single-use strategies and tools are constantly evolving to better serve industry needs, and adept solutions providers can help streamline development with simple, custom adaptations.

Traditional biomanufacturing relies too heavily on trial and error. By integrating AI and mechanistic models into early design, developers can overcome productivity limits and accelerate timelines.

Watch to discover transformative opportunities and trends in the Life Sciences industry, as well as how to unify digital quality in manufacturing processes to stay ahead in this dynamic field.

LETI-101 uses AAV5 to deliver a compact CRISPR system for allele-selective editing of mutant HTT, showing promise as a one-time treatment for Huntington’s disease with safety and efficacy.

Examine how CDMOs can modernize operations, safeguard data integrity, and improve audit readiness with practical strategies for connecting systems and reducing validation burdens.

Continuous manufacturing delivers agility and precision for pharma, combining automation, reduced manual steps, and quality control to meet regulatory and cost pressures while accelerating development.

Scaling autologous CGTs requires more than technology—it demands digital precision. Learn how life sciences leaders are building future-ready manufacturing environments with advanced digital strategies.

Explore how digital biomanufacturing is revolutionizing drug production by exploring strategies for integrating digital technologies to enhance efficiency and innovation in bioprocessing workflows.

Uncover a Disposable Pen for Semaglutide that is a generic drug-device combination, designed for usability and regulatory compliance, showing comparable performance to the reference device.

Find out how eValidation revolutionizes the pharmaceutical industry by enhancing compliance, efficiency, and data integrity, as well as its indispensable role in modernizing traditional validation methods.

AI-powered predictive maintenance with wireless vibration sensors prevented costly batch loss and production shutdowns in manufacturing by detecting equipment issues before failures occurred.

True digital twins are redefining pharmaceutical manufacturing. Review key distinctions, GMP-aligned frameworks, and real-world applications in predictive quality, CPV, and intelligent optimization.

Automation enhances efficiency and minimizes contamination risks and labor costs. Despite the initial investment in automation equipment, the long-term savings can be significant.

Transferring visual inspection data from paper to digital is essential for Pharma 4.0 compliance. Delve into practical strategies to eliminate errors, automate data tracking, and enhance quality.