Our services as a Contract Development and Manufacturing Organization (CDMO) are tailored to support pharmaceutical and biotechnology companies in bringing their products from concept to market. We offer a comprehensive range of services that encompass every stage of the development and manufacturing process. This includes drug formulation, where we assist in designing the optimal composition of a drug, and process development, where we establish and refine the methods for producing these products at scale. Our manufacturing capabilities are built to GMP standards, ensuring that all products are produced with the highest levels of quality, safety, and compliance. We specialize in the production of biologics, including stem cells, gene therapies, and other advanced therapeutics. Our facility is equipped to handle both small-scale clinical batches and large-scale commercial production, offering flexibility to meet the varying needs of our clients. In addition to manufacturing, we provide regulatory support to help navigate the complex approval processes required by Indonesia health authorities. Our team works closely with clients to ensure that all necessary documentation and quality standards are met. We also offer analytical and quality control services, providing thorough testing and validation to ensure the efficacy and safety of the products. By offering end-to-end CDMO services, we enable our clients to focus on their core strengths in research and innovation while we manage the complexities of product development and manufacturing, helping to bring new therapies to patients more efficiently and effectively.