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ABOUT Simson API

Simson API was established in 2023 as a vertically integrated manufacturer of APIs and intermediates. The company operates under Simson Pharma, a privately owned leader in pharmaceutical reference standards founded in 2011. Driven by a strong commitment to innovation, Simson API leverages extensive research and development capabilities along with a highly skilled workforce to deliver a broad range of chemistry solutions. Our expertise spans custom synthesis, process research, and large-scale manufacturing, supporting pharmaceutical companies worldwide with reliable, high-quality services.

OUR VISION

To be a global leader in the development and supply of high-quality, innovative, and sustainable active pharmaceutical ingredients, empowering healthcare providers to improve patient outcomes worldwide

OUR MISSION

To manufacture high-quality, sustainable active pharmaceutical ingredients that exceed customer expectations through rigorous quality control, eco-friendly practices, and a customer-focused approach, ensuring reliable supply and contributing to the success of our partners in delivering safe and effective medicines to improve global health.

CDMO Services

Synthesis & Development

Small and complex molecule synthesis and analytical development with emphasis on speed, flexibility, and quality.

Early Phase Studies

Early phase chemistry development studies, stability studies, and scale-up.

Contract Manufacturing

Contract development and cGMP manufacturing to ensure high standards.

Custom Synthesis

Custom synthesis of peptides and amino acids tailored to your needs.

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