For Registration Campaign and Process Validation, we have a flexible late-phase approach, depending on customer requirements; with an up-front strategy, created and tailored along with our customers, based on sensitivity to risk & overall cost. Our methodology and process is fully compliant with ICH Q7, 8, 9, 10 & 11 and follows a Quality by Design programme, including PAR (Proven Acceptable Ranges) studies.
We systematically screen the important process parameters through optimization and process characterization, by statistical DoE (design of experiments) and each project is subject to rigorous product quality risk assessments. Lifecycles are validated according to FDA guidelines.
Our teams generate all supporting data for filing, including synthesis & characterization of analytical standards, forced degradation studies, stability data & others as required for each project, including late phase Documentation (PPA, QRIA, PAR, Process Summary, PV, PQR- Reports).