Manufacturing reliable healthcare solutions
to improve people’s lives

We provide high-quality and safe generic drugs to more than 40 countries across major continents, made possible by our rapid generic drug development and competent contract research services.

We implement a distinct and smooth process that entails intensive R&D, well-structured scaling up, contract manufacturing to enhance overall productivity, and rigorous clinical trials for ensuring safety evaluation. All these steps ultimately lead to reliable commercial manufacturing.

In order to critically evaluate product-specific acceptance criteria and achieve accurate results, we implement the analytical method of drug development followed by the required validation procedures.

We identify product potential, enabling us to devise innovative process solutions. After this, we proceed with product approvals, eventually leading to an ANDA filing with the FDA.

We have developed financially-prudent high-efficiency methods to innovate IP-oriented formulations. We also economize the development of process technologies.

All through the development process, our knowledgeable regulatory teams conduct periodic quality checks to ensure that our complex generics are highly efficacious. Strong API manufacturers support our formulation development, ensuring that our medicinal supply remains stable and consistent for the foreseeable future.