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We have plentiful resources of the QSR compliant, GMP, ISO9001, and ISO13485 certified manufacturers that generate high-volume and cost-effective syringes to satisfy the need of the healthcare market. ABCorp also provides a full-spectrum consultation service for the prototype device design, product manufacturing, and marketing strategies to assist market penetration of the products. In addition, we offer consulting services in quality and regulatory compliance for medical devices, including FDA 21 CFR 820 (QSR / cGMP), FDA 510(k) pre-market notification, and European Union CE marking& regulatory compliance. Serving as a registered US agent, ABCorp helps foreign manufacturers / establishments that import products to the USA, communicate with FDA and its inquiries. Please contact us for service inquires! |
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