IBL Group Quality Policy
- We always put forth our best efforts to provide our high quality products and services to our customers.
- 1. We always pursue safety, stability, and accuracy in product manufacturing.
- 2. We always put forth our best efforts for our quality improvement based on customer needs in a serious manner with sincerity.
- 3. We place importance on compliance and adhere to regulatory requirements and laws and regulations.
ISO 13485
Antibody related Business at IBL maximize the know-how and expertise in antibody development and production we have gained over the years in line with our corporate policy. At the division of IBL, we are always working to improve and maintain the validity of our quality management system in compliance with laws and regulations, ensuring that we can provide high-quality products to customers around the world. We have obtained ISO 13485 certification, which is the global standard quality management system in the medical field for maintaining, manufacturing, and providing safe and valuable medical equipment.
Scope of Certification
・Design and development, and manufacture of In Vitro Diagnostic Reagents for Immunoassay.
・Manufacture of Materials of In Vitro Diagnostic Reagents for Immunoassay.
