EXPERIENCED AND REGULATION COMPLIANCE
Cosmos Biomed Consulting was established in 2018. The main members of the team are from global CRO company. The service portfolio covered most biotechnology industries such as medical devices, pharmaceuticals, and functional health foods. The team members have an average of more than 10 years working experience. In addition, it is also composed of well-known medical device expert who familiar with US FDA, European CE mark and China NMPA regulation and registration process.
STAND SHANGHAI , SERVICE GLOBAL
China, the most growth market of medical device around the world, especially Shanghai, most medical device company setup. Due to medical device industry of China face rapidly regulation change and demand for professional testing service, Cosmos Biomed established Shanghai office in 2018. We provide oversea regulation consulting service to China and global company in this China Economic and Trade Center. Through our team professional services, we assist the products submission license quickly and complete the test verification and obtain the license. In addition, Cosmos Biomed cooperate with Leon OECD GLP to extend the years of testing services and regulatory experience to become the best bridge between a medical device manufacturer to enter the Chinese market or international market.
COMPLIANCE EFFIENCIENCY AND WIN-WIN
Cosmos Biomed core spirit are three major objectives: “Compliance, Efficiency, and Win-Win”. In addition to our medical device regulatory consulting team and we integrated medical device regulatory consulting service platform to enable our customers enter the world market at any time. Medical device regulations service reduces development time costs and provide one-stop high-efficiency services from sterilization, animal testing strategy and product registration. We have a world-class OECD GLP animal laboratory with more than 1,500 pre-clinical testing projects so far and we have also established long-term strategic cooperation with cross-strait testing and certification agencies and experts to assist Chinese NMPA, EU CE and US FDA registration services. Cosmos Biomed own comprehensive consulting and integrated service platform helps customers to quickly gain the pre-market permission. “We believe that service is not just a trust, but a responsibility for product rigor.” We have been instructed to obtain international registration licenses for many global medical device companies and look forward to working with national partners to create a golden age of biotechnology through our professional services.