Our quality management program covers every phase of product implementation - from conception to design to manufacturing and to delivery. The products developed by I-SEE should pass the tests of cytotoxicity, sensitization, irritation, extraction, clinic, and others.

For the highest accuracy and precision, I-SEE adopts the most sophisticated machineries and equipments producing quality and excellence. We also integrate automatic inspection system with highly trained QC inspectors to ensure the ultimate superior products. As a result, our products are accorded with the MIL-STD 105E international inspection standards and I-SEE has obtained the CE Mark and ISO13485 certifications, and the GMP certification issued by the Bureau of Health in Taiwan, and an approved foreign medical device manufacturer from MHLW of Japan. These certifications stand and prove I-SEE's efforts and insistence of product quality.

We will continue to keep abreast to the newest standard and focus on a customer-oriented quality assurance strategy, while maintaining a policy of “customer satisfaction as the first priority”.