• Do you provide toxicology, safety assessment, or GLP studies?
    Yes. Leadgene Group’s subsidiary, SIDSCO, is a TAF-certified, GLP-compliant laboratory authorized to conduct toxicity and safety studies for pharmaceuticals, health foods, and regenerative medicine products. The study scope and regulatory requirements for GLP studies are evaluated based on your product type and development stage.
    What information is required to evaluate a preclinical study project, and what reports and data will I receive?
    To help us evaluate your project, feel free to share your research objectives, study requirements, testing needs, and expected outcomes. Leadgene Group’s subsidiary, SIDSCO, will then discuss your needs with you and design an experimental workflow tailored to your project requirements. Experimental progress updates, data, and image information will be provided during the study, followed by a complete formal study report and results upon project completion. Additionally, SIDSCO offers a cloud-based system allowing you to access study plans, data, images, and reports online at any time