ARC Trademark

Education services, namely, providing training courses, online and live classes, seminars, webinars, workshops and tutorials in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; providing of training in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; education services in the medical and life sciences industries; educational services in relation to regulatory compliance, issues, updates and developments; educational services in relation to data integrity, unique device identification and regulatory readiness; education and training in relation to compliance and legal aspects of the European union In vitro Diagnostic Regulation; education services relating to quality services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; legal education services; publication of instructional literature, none of the foregoing in connection with the travel industry; publishing, reporting, and writing of texts, other than publicity texts, none of the foregoing in connection with the travel industry; arranging and conducting conferences, workshops, seminars, symposium, competitions, conventions and meetings in the medical and life sciences industries; writing, reporting and publication of non-downloadable guidelines, reports, data and case studies relating to the medical and life sciences industries; advisory and consultancy services relating to all abovementioned services; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector.

Computers, computer hardware and computer peripheral devices; computer software, computer application software, application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; Computer software, computer application software, application software for mobile devices, all of the aforesaid being downloadable or recorded and for the purpose of delivering training and educational content in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded computer software for generating reports concerning regulatory requirements in the medical and life sciences industries; downloadable and recorded computer software for delivering training in relation to regulatory requirements in the medical and life sciences industries; downloadable publications, namely, magazines, newsletters, periodicals and brochures, all in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable and recorded media including written, image, video, audio and visual content, and infographics, namely e-books, CDs, DVDs, audio and video recordings, digital image files, podcasts and webinars in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; downloadable toolkits containing education, teaching and training resources comprised of downloadable guidelines, reports and data relating to regulatory compliance in the medical and life sciences industries; downloadable guidelines, reports and data relating to regulatory compliance in the medical and life sciences industries; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector; none of the aforesaid in relation to the manufacture, provision, or supply of microprocessors, motherboard chipsets, network interface controllers and integrated circuits, flash memory, graphics chips, embedded processors nor other devices or software related to electronic design automation solutions and services

Clinical medical consultation services; medical information; professional consultancy relating to health care; advisory services relating to medical and surgical instruments and devices; consulting and advisory services relating to obtaining and maintaining commerical product certifications for medical and surgical instruments and devices; consultancy and information services relating to medical, pharmaceutical and biopharmaceutical products; consulting and advisory services relating to the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to the European Union medical device regulation (MDR); consulting and advisory services relating to medical aspects of the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to medical aspects of the European Union medical device regulation (MDR); preparation of reports relating to medical matters; preparation of clinical and performance evaluation reports; preparation of clinical and performance evaluation reports for medical devices; information, consultancy and advisory services relating to all above mentioned services.

Business organization and administration, none of the foregoing in connection with the travel industry; providing office functions, none of the foregoing in connection with the travel industry; collection, compilation, analysis, reporting and dissemination of statistics, data and information, none of the foregoing in connection with the travel industry; 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; regulatory submission management, namely, assisting others in preparing and filing applications for regulatory approval of medical devices, medical technologies, medications, pharmaceuticals, and biotechnology; providing information online regarding preparing and filing applications for regulatory submission management; business and advisory consultancy services relating to obtaining and maintaining commercial product certifications

Scientific, technological and industrial analysis, research and design services in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; conducting and designing clinical trials for others; laboratory testing of materials; consultancy services related to laboratory testing of materials; clinical research in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and legal industries; biological research and medical research; site monitoring services; conducting early evaluations in the field of new pharmaceuticals; pharmaceutical product evaluation; product quality evaluation; quality control services for others; quality management services, namely, quality evaluation and analysis, quality assurance and quality control in the medical and life sciences industries; scientific research, analysis, testing, and related scientific studies in the medical and life sciences industries; consulting services in the medical and life sciences industries; biotechnology, biotechnology research consulting services; pharmaceutical research and product development for use in manufacturing; consulting services for others in the field of designing pre-clinical and clinical studies and trials for others; technical writing; technical writing for others; testing, analysis and evaluation of the services of others for the purpose of certification; testing of apparatus in the field of medical devices for certification purposes; electronic data storage; software as a service [SaaS] for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software as a service [SaaS] for the purpose of delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose of accessing, navigating, analysing, updating and identifying regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; providing online, non-downloadable software for the purpose of delivering training, educational content and reports in respect of regulatory and legislative requirements in the field of medicine, life sciences, pharmaceuticals, laboratory research, laboratory testing and law; software design, development and engineering, none of the foregoing in connection with the travel industry; computer software consultancy, none of the foregoing in connection with the travel industry; providing online, nondownloadable software for generating reports concerning regulatory requirements in the medical and life sciences industries; providing online, non-downloadable software for delivering training in relation to regulatory requirements in the medical and life sciences industries; information, consultancy and advisory services relating to all abovementioned services; none of the aforesaid relating to betting or gambling services; none of the aforesaid relating to AI technology specifically used in relation to player protection technology or risk reduction technology in the betting and gambling sector; none of the foresaid in relation to the manufacture, provision, or supply of microprocessors, motherboard chipsets, network interface controllers and integrated circuits, flash memory, graphics chips, embedded processors nor other devices or software related to electronic design automation solutions and services.

Legal services; regulatory and legal compliance auditing; advisory services relating to regulatory affairs; expert consultancy relating to legal issues regulatory compliance consulting services in the life sciences fields; regulatory compliance consulting services in the life sciences fields namely, reviewing standards and practices to assist others with compliance with governmental laws, regulations and rules pertaining to medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; consulting and advisory services relating to legal aspects of the European Union in vitro diagnostic regulation (IVDR); consulting and advisory services relating to legal aspects of the European Union medical device regulation (MDR); legal support services; information, consultancy and advisory services relating to all above mentioned services.