Description: Class 35: Regulatory submission management, namely, assisting others in preparing and filing applications for new medical devices with governmental regulatory bodies
Class 42: Pharmaceutical, medical, and scientific research services; Pharmaceutical drug development and discovery services; Medical laboratory research services; Scientific laboratory services; Preclinical services, namely, medical research laboratory services in the fields of pharmacology, pharmacokinetics, and toxicology in well-established lab animal models; Scientific research and development services for bioanalytical testing; Quality control services, namely, calibration and measurement capability (CMC) laboratory and stability testing; Providing laboratory research services for others in the fields of pharmaceuticals, medical devices, histopathology; Research and development in the fields of production and analysis of viral-based vectors, pharmaceuticals, biologics, vaccines, biotechnological products, and gene and cell therapy preparations; Pharmaceutical research and development; Preclinical pharmaceutical research, pharmaceutical clinical research, pre-clinical pharmaceutical testing, and providing in vitro testing for pharmaceutical product research, discovery, and development; Designing clinical trials for others; Developing regulatory and product development strategies, Scientific research in the nature of conducting clinical trials for others; Testing of pharmaceuticals of others; Testing of medical devices for others
