06.21.22 -- SimpliFiH Solutions For Accelerated Pharmaceutical Development

Explore an integrated service package designed to simplify and accelerate the development pathway, even for APIs with challenging properties such as low aqueous solubility and poor bioavailability.

Lonza’s Ibex Design workflow's process platforms, straightforward scale-up to cGMP manufacturing, and innovative technologies further reduce development time and improve overall productivity.

In this technical note, we demonstrate parallel, highly reproducible capillary isoelectric focusing analysis using a multicapillary separation approach to accelerate analysis time.

Understand how the supply chain experience, severely affected by COVID-19, involving global workforce disruption, surging demand, and drug shortage notices, is shaping attitudes toward resilience.

Human PSC-derived organoids have a promising future in many research and biomedical endeavors — from drug discovery to developmental biology.

A pharmaceutical company sought a development and manufacturing partner to assist with an in-licensed product originating from an emerging pharma company, a molecule in clinical Phase 2/3 trials.

The successful transition from initial synthesis of an API to a kilogram-scale route requires expert analysis and design and a balance of economic, regulatory, and time constraints.

Choosing the right tag is essential to getting the purity, solubility, and protein quality your application needs. Learn how to prepare a recombinant protein in the quantity and quality you need.