GoBroad Clinical Research Center provides medical writing services covering the lifecycle of drug clinical development. Our team members hold master's degrees or above in medical or biomedical-related subjects and have years of working experience in the industry. With established robust processes and quality management system, we offer clients writing services of clinical trial protocols, informed consent forms, clinical trial reports, investigator brochures, and other clinical documents required from the Investigational New Drug (IND) through New Drug Application (NDA). Our services comply with ICH and regulatory requirements of main countries. We have experience in writing submission documents for drug registration in both China and the US for many clients.