Tetra Med Sciences offers integrated and standalone drug development solutions to suit customer requirements in different stages of preclinical and clinical development. We provide non-GMP/GMP grade key starting materials (KSMs), advanced intermediates and active pharmaceutical ingredients (APIs) in required quantities, from kilo laboratory to plant scale.

With a flexible and innovation mindset, and hands-on experience in a variety of chemistries, we proactively address potential challenges in early or late development. This ensures successful technology transfer from preclinical supply and late stage development, to commercial manufacturing. The team leverages learnings from diverse projects to accelerate the overall development timelines of every new project. We support customer needs to efficiently manage their development projects from IND-enabling pharm-tox stage to global clinical trials.

Seamlessly accelerating drug manufacturing across the development continuum

    Tetra Med Sciences experienced process chemists, process engineers, analytical scientists, safety professionals, and manufacturing experts
    with an unparalleled track record.

    Our scientists have significant training and experience across synthetic organic chemistry, analytical chemistry, process chemistry, process safety, and engineering.

    The chemical development team is supported by experts from our supply chain, warehouse, quality control, and quality assurance teams.

    Our state-of-the-art process engineering and process safety laboratories, help in making processes rich with scientific data for execution at every scale.