Nitto Denko is engaged in the development of products based on the application of polymer materials. These include transdermal pharmaceutics and other pharmaceutical products and wound-dressing materials and other medical devices and products. As these products are used in direct contact with the human body, biological evaluations are applied to ensure their safety and efficacy.
For pharmaceutical products and medical devices, in order to design products that combine safety with efficacy, the safety of drugs, additives (e.g. adhesives), and other raw materials and the safety of the products is evaluated in accordance with GLP standards and with toxicity study guidelines. For medical products, safety evaluation in line with the individual characteristics of the product is carried out with reference to the Product Liability Law.
Safety Evaluation of Pharmaceutical Products
Pharmaceutical products are subject to biological evaluation from the product design stage aimed at ensuring safety.
General toxicity study (single-dose toxicity, repeated-dose toxicity) (rat, mouse)
Mutagenicity studies (bacteria, cultured cells, rat, mouse)
Skin sensitization study, phototoxicity study, photosensitization study (guinea pig)
Intracutaneous reaction study (rabbit)
Safety Evaluation of Medical Devices and Products
For wound-dressing materials, large first-aid bandages, surgical tape, and similar products, biological evaluation of safety and usefulness is carried out in line with the specific applications and characteristics of the product.
・Single-dose toxicity study (rat, mouse)
・Primary skin irritation study (rabbit)
・Skin sensitization study (guinea pig)
・Intracutaneous reaction study (rabbit)
Cytotoxicity (cultured cells)
Biocompatibility study (rat, rabbit, etc.)
Wound-healing study (rat, rabbit, etc.)
For any inquiries about R&D.
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