Our mission is to ensure the generation of accurate and precise findings.
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At Auxiliary Biosciences, we provide custom synthesis services tailored to your needs. Leveraging established literature protocols or developing new, efficient routes, we ensure rapid and reliable production of target molecules. Our commitment to precision and innovation accelerates your research and development timelines. Beyond small-scale synthesis, Auxiliary excels in scale-up capabilities, providing kilogram quantities to precisely meet our clients' requirements.
Specializing in, yet not limited to:
Our expertise includes, but not limited to:
• Molecule Synthesis: Custom synthesis of molecules, from basic to complex.
• Medicinal Chemistry Solutions: Optimize drug discovery through refined synthesis processes.
• Process Development: APIs and their intermediates.
• Reference compounds for research and compliance: APIs, API impurities, and drug metabolites
• Isotope-labelled analogues.
• Peptide Synthesis: Liquid and solid phase peptide synthesis
• Agrochemicals.
At Auxiliary Biosciences, we offer end-to-end services for active pharmaceutical ingredient (API) development and manufacturing. Our expert chemists utilize modern tools for route scouting to design, and optimized synthetic processes. We then conduct rigorous process R&D, validation and scale up under cGMP conditions. Clients benefit from our flexibility in custom API production across diverse routes. As a reliable manufacturing partner, we provide drug substance clinical trial material and commercial supplies. Contact us to discuss your API needs and compatible timelines.
Our engineers and scientists specialize in process development and manufacturing technologies. Through cutting-edge methods like continuous flow synthesis, we rapidly design and validate efficient production routes. We employ leading chemistry and engineering practices to manufacture your molecules reproducibly under the highest quality and safety standards. By partnering with us, companies gain fast access to well-characterized commercial processes. Learn how our integrated expertise streamlines facility transfers and supply.
We conduct thorough evaluations adhering to global guidance like HazOp. Our toxicologists characterize the hazards involved and assess risks to develop robust controls. Through meticulous stability protocols, we assure your substances maintain integrity over their entire shelf life. Clients benefit from our scientific rigor that protects people and the environment. Discuss with us how we can enable your full process safety profile.
Our innovation-focused projects advance the frontiers of API manufacture. Our Flow Chemistry Centers enable improved productivity and control over batch operations. Expertise in alternative technologies like microwave synthesis provides greener production routes. As pioneers in process automation, we partner flexibly across scales from bench to commercial scale. Contact us for innovative solutions that optimize your route efficiency and sustainability.
State-of-the-art characterization of formulation behaviors shortens development time. Scale-up of finished dosage forms like tablets, capsules and injectables aligns seamlessly with regulatory requirements. Our Dissolution and Stability programs substantiate shelf life claims. Choose us to de-risk product development uncertainties and accelerate program launches.
We apply a rigorous multidisciplinary approach from method establishment through validation and compliant testing. Our expertise encompasses analysis of chemical compounds with diverse analytical techniques, interpretation, characterization and data report. Through custom project planning, we deliver dependable results traceable to global standards. Engage us to maximize analytical efficiency for your submissions and production monitoring.
We offer integrated drug discovery services to support our partners in early stage development. Using medicinal chemistry expertise, our team works to identify potential candidates through hit identification, optimization and profiling. With experience across multiple therapeutic areas, we aim to progress efficiently. We design tailored discovery plans leveraging compound libraries, structural analysis techniques and ADME profiling. Experienced scientists utilize cutting-edge technologies to evaluate molecules and select leads. Our data-driven approach identifies candidates with desirable characteristics for further testing. Backed by skilled teams and state-of-the-art infrastructure, we address our client's discovery objectives rapidly and strategically. Partner with our discovery experts to identify safe and effective preclinical assets primed for development studies within your timeframe and budget. Our integrated solutions enhance your early research goals.
Our IPR experts secure intellectual property assets related to research, development, and manufacturing activities. This encompasses securing patents, trademarks, and copyrights to protect proprietary technologies, inventions, novel subject matters of medicinal compounds, active pharmaceutical ingredients, and product formulations. Aditionally, we offer consulting and advisory services to clients seeking guidance on various aspects of portfolio such as product selection, brief patent landscapes,literature reports, patentability evaluation for the inventions, freedom to operate opinions, filing and patent management, trademark filing and maintaining activities, opinion on legal related matters.