DRA

Owner

Goods & Services

Consulting services in the field of medical product approval for commercial purposes; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing independent review of clinical trials for business purposes; Business consultancy relating to regulatory compliance; Regulatory submission management, namely, assisting others in preparing and filing applications for medical devices with governmental regulatory bodies

Providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; Regulatory compliance consulting in the field of pharmaceuticals, medical devices, and clinical research

Consulting services for others in the field of design, planning, and implementation project management of scientific research and clinical trials; Providing medical and scientific research information in the field of pharmaceuticals and clinical trials; Monitoring clinical research for quality control purposes; Monitoring the manufacture of pharmaceuticals and medical devices for quality control purposes