Contract Manufacturing

From Discovery to Delivery: Expertise Across the Drug Lifecycle

As a leading Contract Development and Manufacturing Organization (CDMO) and an integral part of Troikaa Pharmaceuticals Ltd., Troikaa Pharmachem Pvt. Ltd. offers comprehensive, end-to-end development and manufacturing solutions across the entire drug lifecycle. We are committed to delivering high-quality services that streamline your product development and manufacturing needs.

Our offerings span a broad range of services, including drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, and commercial supply of both Active Pharmaceutical Ingredients (APIs) and finished dosage forms. We also specialize in advanced services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products, and potent solid oral drug formulations.

Customized Contract Manufacturing for Every Stage

Expertise in Complex Solutions

Our dedicated team is proficient in developing small-molecule Novel Chemical Entities (NCEs) with precision, adhering to the highest quality standards. With extensive experience across diverse methodologies, we specialize in the synthesis of single compounds, multi-step processes, small arrays, and focused libraries. Our scientific team excels in constructing parallel focused libraries, facilitating hit-to-lead and lead optimization projects.

Scalable and Flexible Manufacturing

We pride ourselves on offering unparalleled flexibility in scaling production up or down to meet demand, empowering our clients to adapt swiftly to market changes. Whether you need small batches or large-scale manufacturing, our capabilities allow you to respond without the burden of excess capacity. By leveraging our resources, expertise, and infrastructure, you can expedite your production timelines and bring innovative products to market faster

Quality and Regulatory Excellence

we adhere to the strictest global standards of regulatory compliance and quality assurance. Our facilities operate under cGMP guidelines, ensuring that every product is manufactured to the highest level of safety, efficacy, and consistency. This commitment to quality extends throughout the entire drug development process, giving our clients peace of mind as they navigate the complexities of bringing new products to market.