VIPL strongly believes that with its excellent infrastructure and extensive chemical business background, it is aptly positioned for APIs & Intermediates manufacturing and outsourcing for global pharmaceutical & chemical industries.
The ultimate business strategy of VIPL is “ to be a partner in the global pharmaceutical and chemical industries and continue to be a reliable and consistent supplier of APIs and Intermediates”.
APIs and Intermediates
VIPL has built up strength in the development, process optimization, scale-up and cGMP production of APIs and Intermediates.
The company carefully analyses & evaluates Intellectual Property Rights (IPR) to avoid patent infringement.
VIPL capabilities include non-infringing synthetic route selection with respect to patents, processes and analytical validation, optimization and successful scale-up from bench to manufacturing. Production is undertaken in the state-of-the-art multi-purpose cGMP compliant manufacturing facility. In order to meet the regulatory requirements, molecule formation, isolation of API and their subsequent operations such as drying, milling, blending and packing are carried out in a facility having cGMP practices.
VIPL has a large intermediate plant capable of handling complex reactions and has the capability of manufacturing as per customer requirements.