Biovedic Life Sciences provides both integrated and standalone drug development solutions tailored to customer needs at various stages of preclinical and clinical development. We supply key starting materials (KSMs), advanced intermediates, and active pharmaceutical ingredients (APIs) in the required quantities, ranging from kilo laboratory to plant scale, with both non-GMP and GMP options available.


With a flexible and innovative approach, combined with hands-on experience in various chemistries, we proactively tackle potential challenges during both early and late development phases. This ensures smooth technology transfer from preclinical supply and late-stage development to commercial manufacturing. Our team leverages insights from diverse projects to accelerate overall development timelines for every new initiative. We also support our customers in efficiently managing their development projects, from the IND-enabling pharmacotoxicology stage to global clinical trials.

Effortlessly accelerating drug manufacturing throughout the development continuum.

    Biovedic Life Sciences boasts a team of experienced process chemists, process engineers, analytical scientists, safety professionals, and manufacturing experts, all with an exceptional track record.

    Our scientists possess extensive training and experience in synthetic organic chemistry, analytical chemistry, process chemistry, process safety, and engineering.

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

    Our state-of-the-art process engineering and process safety laboratories generate scientifically robust data to facilitate execution at every scale.