06.10.25 -- Understanding The Impact Of An RMP On Patient Risks Using Relational Risk Analysis

The following insights and case studies demonstrate how a tailored, stepwise testing approach can effectively detect, quantify, and control nitrosamine impurities while maintaining cost efficiency.

Leveraging computer-aided synthesis design technology and route scouting in the early stages of development can aid you in designing an efficient and cost-effective path to API manufacturing.

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.

Explore how Dr. Shehaab Savliwala, a leading formulation scientist at Singota Solutions, transforms complex pharmaceutical challenges into breakthroughs and innovative drug delivery.

Discover groundbreaking data that supports the use of the Sinclair Nanopig to reduce reliance on traditional non-rodent species in drug development, validating its value in drug safety studies.