retesting of raw materials in pharmaceuticals - 0 views
-
crystalpharmate on 31 Jul 24We will provide our valued customers with analytical chemistry testing research and quality control services for NCEs throughout their life cycle from the early clinical stage to commercial manufacturing. Analytical Method Development and Validation Guided by Quality by Design (QbD), we provide comprehensive analytical method development and validation in accordance with ICH Q2 based on Critical Quality Attributes (CQA) to support oral dosage form development. We also perform life cycle management to ensure quality research and control and provide accurate and reliable data at different drug development stages.