Method Development and Validation

Solvias utilizes the latest technologies for micro analytical, physical chemistry and separation techniques. These technologies are applied to develop and validate methods for release testing and cleaning validations. In accordance to current ICH-guidelines, projects in the field of toxicological and clinical studies, pharmaceutical R & D and quality control are supported.

We create SOP’s and provide GMP validation protocols and reports according to our customer specifications and needs.
This service is also extended to computerized systems to ensure your compliance with 21 CFR Part 11.

If you need assistance for production, our custom process analysers are provided with full validation services in order to make them congruent with your process control systems.