Description: Class 35: Regulatory submission management, namely, assisting others in preparing and filing applications for pharmaceuticals and medical devices with governmental regulatory bodies; 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; Providing independent review of clinical trials for business purposes
Class 42: Laboratory analysis in the field of microbiology, biocompatibility, toxicology, chemistry, cosmetics, medical devices, pharmaceuticals, consumer products, vitamins and dietary supplements, food and beverages, and tissues; Scientific research consulting in the field of in the field of laboratory diagnostics, microbiological studies, chemical synthesis, chemical formulation, and environmental monitoring to verify cleaning and sanitization; 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
Class 45: Regulatory compliance auditing; Regulatory compliance consulting in the field of pharmaceuticals and medical devices; 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
