Analytical Support 

The analytical experts at Societal CDMO San Diego possess the technical skills, equipment, and experience necessary to develop and validate analytical methods, cGMP testing, and stability assessments to support your pharmaceutical finished product.

Our pharmaceutical analytical development and testing services cover the characterization of physicochemical properties during pre-formulation to performing commercial quality control (QC) release testing for both raw materials and various types of finished products.

We have created and verified analytical methods for various pharmaceutical products. These methods facilitate the characterization and performance or stability testing of finished products, ensuring compliance with the requirements for drug release in GMP clinical and commercial manufacturing.

TPP possesses the expertise and capabilities for analytical method development, validation, and testing to support every pharmaceutical development and testing phase, from pre-formulation studies to commercial products. We employ a systematic scientific approach tailored to each development phase. Our team adheres to the global guidelines established by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) to guarantee high-quality pharmaceutical products with the required potency, purity, and performance.