GoBroad Clinical Research Center provides regulatory consulting services for pharmaceutical product registration. We are committed to helping clients in accelerating the development and market authorization application of pharmaceutical products. Our team are well-versed in the process and technical requirements of drug development, having in-depth understanding of the drug registration regulations.

We accurately profile the characteristics of products and integrate both internal and external expertise within the GoBroad Group, including but not limited to Principal Investigators (PI), regulatory consultants, clinical pharmacologists, medical experts, and statisticians. This enables us to assess the feasibility and gaps in drug registration, identify risks, and provide consulting services on regulatory affairs, clinical development pathways, and registration application strategies through a multidisciplinary approach, assisting clients in setting up customized and differentiated product development strategies.