Class [42]
Computer & Software Services & Scientific Services
Design, maintenance, development, updating, and upgrading of computer software; computer software development in the field of regulated industries, namely, medical devices, in-vitro diagnostics, pharmaceuticals, biologics, and dental; design and development of computer software for creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; customizing computer software by creating user and company specific alerts for expiring regulatory registrations, changes to regulatory information, and events on economic, legislative, and regulatory developments as it relates to and can impact businesses; maintenance of computer software used for creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; providing a website featuring on-line non-downloadable software that enables users to create, edit, and maintain regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; providing temporary use of a web-based software application for creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; providing temporary use of non-downloadable cloud-based software for creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; cloud computing featuring software for use creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; technical support services, namely, troubleshooting of computer software problems, and installation, administration, and troubleshooting of web and database applications; software as a service (SAAS) services featuring software for regulated industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; application service provider (ASP) featuring software for use in creating, editing, and maintaining regulatory intelligence, public and private information, open-source resources, and proprietary connection points within a database for industries associated with medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries.
Class [45]
Personal & Legal & Social Services
Regulatory compliance consulting in the field of medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated industries; Tracking and monitoring regulatory requirements in the field of medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, cannabis, and other regulated industries for regulatory compliance purposes; Computer software licensing; Regulatory submission management, namely, assisting others in preparing and filing applications for medical devices, in-vitro diagnostics, pharmaceuticals, biologics, dental, and other regulated products 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; providing information and news on legislative, and regulatory developments as it relates to and can impact businesses; 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; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs with governmental regulatory bodies.
