RESEARCH & DEVELOPMENT

With expertise in generics drug product research and development, formulation manufacturing, latest quality movements, and in-depth insight into the international pharmaceuticals markets, continuous efforts are made to offer solutions that give an extra advantage to our Partners. The key to our success is being able to offer a flexible approach whether it is a:

* step-by-step development work, providing scientific and technical expertise about technologically advanced CRO and CMO facilities, manufacturing know how, analysis of molecule stability testing data, evaluation of BA/BE clinical study data, etc...; or

* transfer of a complete product dossier quickly and at a reasonable cost. More importantly, allowing our Partners to save approximately 12 months in resources and time, while executing our dossier with high certainty of success.

Our work is always performed under the spice of meeting current USP/EP methodologies, ICH Guidelines, QbD, cGMP, and EMEA/FDA regulations, as well as relevant international specifications.

Currently, we have a robust pipeline of injectable and ophthalmic products in a variety of therapeutic classes.