02.26.26 -- At Base Camp: Lilly's Manufacturing Capacity Journey

Bringing complex generics to market requires deep expertise. Learn how a CDMO can help navigate regulatory, technical, and commercial challenges with end-to-end development support.

Discover how Liquid Phase Peptide Synthesis (LPPS) uses traditional reactors to create more efficient and sustainable peptide manufacturing. Learn about key analytical and quality control considerations.

View a study which provides additional insight into the factors that govern the discoloration of protein therapeutics and the role of AGEs in color change.

A majority of methods used to detect pinholes, cracks, and defective seals in containers are destructive. Read about High Voltage Leak Detection (HVLD) and why it is free from these shortcomings.

Explore an array of mixers and mixing technologies that can help you throughout the cannabis product manufacturing process.

Major retailers are mandating x-ray inspection for their suppliers. Uncover why this technology is crucial, and its capabilities beyond contamination detection to encompass vital quality checks.

Lowering EO levels is possible without sacrificing sterility. Find out how calibrated PCDs and precise cycle control can reduce risk and streamline validation for more sustainable sterilization.

More and more industrial gear is hitting the auction block. Unlock significant savings by understanding the nuances of pharmaceutical and industrial equipment auctions.

Review analytical strategies designed to address challenges occurring during development of new molecular formats such as chain assembly, multiple-MoAs, and diverse post-translational modifications.

A recent survey of over 850 biopharma professionals reveals key challenges and priorities for managing lab data, including scalability and improving research efficiency.

See how to select the right lysis reagent, protect protein from degradation, reduce the viscosity of your sample, and determine the μg of protein needed per your final assay.

Effective CCI testing hinges on strategic sampling and statistical rigor. Reveal why 30 samples matter, how positive controls validate defect detection, and why risk assessment ensures long-term reliability.

Closing and following up after a CDMO audit requires organized findings, clear communication, actionable recommendations, and ongoing collaboration to strengthen compliance.

Designed for scientists and engineers evaluating advanced reactors, this recording delivers practical insights and real-world examples to support safer, more efficient, and adaptable flow chemistry.

Strategic equipment relocation and retrofitting can reduce capital costs by fifty percent and save months in lead time. Learn how to modernize legacy systems while maintaining full GMP compliance.