Can Medicilon provide a full range of pre-market services such as medical device registration?

Medisign is a senior brand of medical device registration consulting service in China. Founded in 2011, Medicilon is specialized in providing pre-market services for medical devices and in vitro diagnostic reagents in China. It specializes in providing one-stop pre-market regulatory consulting services for medical devices and in vitro diagnostic reagents in China. The company's core business includes medical device registration, testing agency, clinical trials, clinical evaluation report writing, as well as commissioned manufacturing, quality management system counseling and other services. Our team has more than 100 professional and technical staff from multinational corporations, domestic manufacturers and regulatory consulting organizations. During the 12 years of development, Medisys has always adhered to the attitude and method of continuous learning, unremitting research and continuous improvement, and is committed to providing customers with more comprehensive solutions. Up to now, we have assisted domestic and foreign partner companies to obtain more than 1,500 medical device registration certificates. Medical device clinical trial services have formed industry-leading project experience and resource deposition in the fields of surgical robots, AI software, orthopedic implants and innovative biomaterials, medical cosmetic devices and implants, energy therapy devices, in vitro diagnostic reagents, and medical imaging devices. If you need to outsource processes such as medical device registration and filing, consider consulting with Medisoft first to evaluate and find the best path to market for your product.