Analytical development and Quality Control
Structured. Straightforward. Reliable.
Our analytical experts in Pharmaceutical Sciences take a structured, straightforward and reliable approach to method development and validation. They are delivering effective solutions for all development phases by adhering to Quality by Design (QbD) principles and using latest generation software tools to support both development and validation.
Our consistent software assisted strategy for method development is delivering high performance, robust and reliable stability indicating HPLC methods for any phase of development.
We use fully regulatory compliant and integrated analytical validation software packages to ensure prompt generation and evaluation of data against acceptance criteria, and to guarantee full traceability and secure storage of data (21 CRF Part 11 compliant).
Using method development workstations combined with chromatography modelling software packages and computer assisted method development tools, our expert scientists are supporting the method development strategy and maximizing the output of each experiment. We can provide quick and excellent solutions to any analytical development problem.