ARS AMERICAN REGULATORY SERVICES

Business consulting and management in the field of preclinical trials, namely, preclinical data generation and regulatory submission management on behalf of medical device, pharmaceutical, and biotechnology companies to assist them with preclinical research and regulatory submission for medical product approval for commercial purposes; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for medical device approval