12.04.24 -- Who Handles Maintenance At Your CDMO? You Should Know

Praveen Prasana from Verve Therapeutics, GenSight Biologics' Scott Jeffers, and Vaibhav Patel from the University of Minnesota discuss quality concerns at CDMOs.

Watch as Cambrex experts walk through a variety of technologies and case studies, focusing on LPPS, peptide crystallization, method development for peptide impurity analysis, and more.

To guide a biotech through successful drug development, there are three key areas a CDMO should focus on: equipment and instrumentation, organization and personnel, and systems and processes.

AI applications in medical writing are in their infancy, and the technology suffers several shortcomings including plagiarism, copyright infringement, and misinformation dissemination.

This paper presents three approaches to address poor solubility in organic solvents for spray drying as well as case studies outlining their successful application during development.

With a growing interest in developing new and improved bioconjugate drugs, explore an “innovation through collaboration” approach that can facilitate access to next-generation conjugation technologies.

Discover how nanomilling, a game-changing technique that tackles poor solubility and bioavailability in drug development, can optimize your drug’s formulation.

Review the key trends and challenges shaping the CDMO industry as well as the tools helping a leading CDMO meet the growing demand for pediatric formulations and taste-masking solutions.

Characterizing a molecule's identity enables efficient process development and regulatory compliance. To achieve this, sponsors must leverage analytical techniques that illuminate structure and purity.

Early identification of potential absorption risks is critical for rapid and efficient drug development. Lonza's PBPK modeling services are designed to de-risk your drug development program.

Review our expertise across a wide range of global markets. Our experience in securing regulatory approvals and navigating market challenges positions us as a trusted partner.

Watch this overview of our extensive capabilities, including a deep dive into our HPAPI and API services and the available capacity at our Campoverdi, Italy facility for your next project.

From its facilities in Montreal, Quebec, Ropack handles most paperwork, permissions, components, warehousing, packaging, distribution, collection, and destruction as a single project.