We, at USV constantly endeavour to provide our customers with a consistent quality of products and services. We ensure quality at every step of our manufacturing process right from the sourcing of raw materials from reliable vendors and in-process checks to the finished product. We have established quality management systems that are compliant with cGMP requirements of regulated and semi-regulated markets for drug substance release. Our state-of-the-art facilities are well equipped to conduct method transfers and validations for all batch release parameters of biotherapeutics.

Quality Assurance, as the term suggests, is a commitment towards quality or a set of procedures that are built-in to ensure that the product or service provided will meet required specifications. USV believes in the concept of ‘Building the quality into the product’ by adhering to validated procedures and processes. We have a dedicated team to conduct regular audits of raw material suppliers, pre-clinical and clinical study centers and enforce the implementation of GMP to assure product quality at all stages of product development.

A well defined Quality Policy and Master Validation Plan, in conjunction with a well-trained quality assurance team enable us to assure our customers of products that meet international standards.