Consulting services in the field of U.S. Food and Drug Administration (FDA) regulation and Food and Drug Branch (FDB) regulations; Consulting services in the field of regulatory compliance of products, product packaging and product advertising; Consulting services in the field of regulatory compliance of medical devices; Advisory and consulting services in the field of regulatory submissions and filings for medical devices; Advisory and consulting services in the field of FDA-related submissions, and FDB-related submissions; Advisory and consulting services in the field of product design; Record keeping for regulatory compliance of medical devices; Record keeping of Design History File (DHF), Design History Records (DHR), and Device Master Records (DMR) for regulatory purposes; Business services, namely, FDA-related representation, and FDB-related representation; Business services, namely, hosting medical devices for regulatory purposes; Business services for the commercialization of products; Business services for the commercialization of medical devices; Business services, namely, sourcing of products and services for product development and manufacturing; Business services, namely, monitoring product safety and product efficacy