Support for pharmaceutical development, clinical trials, manufacturing, and quality control.
In clinical trials within the pharmaceutical industry, rigorous testing is required to evaluate the efficacy and safety of drugs. In particular, tests utilizing microorganisms and quality control are crucial elements that influence the reliability of clinical trials. Maple Bio Laboratories leverages microbial control technology to support the necessary testing and research and development for clinical trials. We contribute to solving challenges such as employing full-time researchers, securing research facilities, and reducing development costs. 【Usage Scenarios】 - Antibacterial testing of investigational drugs - Stability testing of investigational drugs - Quality control of investigational drugs 【Benefits of Implementation】 - Improved reliability of clinical trials - Reduction in research and development costs - Increased efficiency in testing and research and development
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【Features】 - Testing and research development using microorganisms - Contract testing for antiviral activity - Preservation efficacy testing (compliant with JP standards, also compatible with USP) - Exploration of antibacterial substances - Microbiome analysis 【Our Strengths】 Since our establishment in 1996, we have a proven track record in contract research and development, with a strong focus on microorganism-related development. We also conduct hygiene management, quality control, and microbiological testing for cosmetic and food factories.
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Since its establishment in 1996, we have been engaged in contract research and development primarily related to biochemistry. Contract research and development: Research and development related to biochemistry (product development, evaluation of product efficacy), fermentation, and development of deodorization-related products. Microbial testing: Hygiene inspections for food factories and cosmetics factories. As an in-house project, we are developing diagnostic and therapeutic agents for muscular dystrophy.
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