The scientific rigor behind the quality standards trusted by manufacturers and regulators around the globe – now available through Ultra Health’s R&D Analytical Solutions  

New manufacturing technologies and increasingly complex drug formulations pose challenges for manufacturers and pharmaceutical companies to bring products to market.  

Ultra Health’s analytical method development and qualification services support in-lab analytical and process development for pharmaceutical R&D. We provide flexible, tailored solutions to help develop and validate* analytical methods, procedures for characterizing drugs and related materials including analytical standards, and methods and processes to identify and control potential impurities.

Method development and validation* and

material characterization services include:

• Identification

• Assays, including stability indicating tests

• Process impurities, residual solvents, potential, mutagenic impurities, and unknowns

• Cleaning validation

• Purity analysis

• Structural characterization

• Material isolation and identification

* Non-GMP, Non-GLP