Service include:
The full implementation of MAH has optimized the allocation of resources, accelerated the listing process of innovative medical device products, and satisfied and promoted the development of medical services. Lu Jian has built a compliant and professional CDMO service platform based on the medical device registrant system, which can provide customers with a one-stop complete solution from concept to product industrialization and compliance listing.
The company could provide R&D services such as process R&D, preparation process optimization, registration inspection, sample production and commercialization customization for products of innovative medical device R&D enterprises and biotechnology companies. At the same time, it can provide supporting services such as legal consultation, system construction, patent application, professional counseling, project incubation, etc. for partners, helping innovative medical device enterprises to reduce R&D production and operation costs, shorten product listing cycle, improve project conversion success rate, improve product registration rate, and efficiently promote the industrialization of medical devices. The platform has independent research and development and production capacity, and has obtained a number of innovative medical device product registration certificates and production licenses.

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