Regulatory affairs

Regulatory affairs services including application of drug import/export license and clinical trials certificate, ethics application and local consent form translation. At CCRB, our regulatory affairs professionals are dedicated to ensure the successful and timely submission of your application. We understand that a poorly prepared submission can result in delayed approval, or even rejection, of your application. We review all submissions for completeness and assemble each submission according to regulatory requirements. We also comply with the changing regulatory guidelines and requirements as well as adapting our services to the emerging trends in submission procedures and technologies. We work closely with you, to determine your specific business needs and to meet your timelines.