• EXPERIENCES

Golden Bridge has established a good corporate reputation overseas derived from its high quality and sincere services. With more than 22 years of experiences in Regulatory Affairs, we have helped hundreds of overseas companies to complete thousands of In Vitro Diagnostic Reagents and Medical Devices products registration, over 725 clinical trials in China, among which, more than 85 products are Class III. All of them meet a variety of In Vitro Diagnostic Reagents and Medical Devices regulation requirements.

 

• PROFESSIONAL TEAM

Golden Bridge consists of over 15 professional and experienced staffs, who are assigned into 3 departments namely Administrative and Finance Department, Regulatory Affair Department, Clinical Department. Our employees possess relative majors and have received specialized training on communication and resolving issue. We all contribute to Golden Bridge high quality services in different ways.

 

• EFFECTIVE COMMUNICATION

Through our long-term experiences in Regulatory Affairs, we’ve obtained a deep, comprehensive understanding on In Vitro Diagnostic Reagents and Medical Devices Laws and Regulations. Based on our long year professional experiences, we have our effective communication and high-efficiency methods to solve problems with China government organizations, such as NMPA, Test Center and Clinical Trial Site.