Mark:

ARC

Status Date:

05-23-2024

Registration Number:

N/A

Goods and Services:

Education; providing of training; 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 GxP (good practice) compliance, risk management, design control, QMS (quality management solutions), SOP (standard operating procedures), data integrity, UDI (unique device identification) and regulatory readiness; education and training in relation to compliance and legal aspects of the European Union in vitro diagnostic regulation (IVDR); education services relating to quality services; legal education services; publication of instructional literature; publishing, reporting, and writing of texts, other than publicity texts; arranging and conducting conferences, workshops, seminars, symposia, 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 above mentioned services. Computers, computer hardware and computer peripheral devices; computer software; computer application software; application software for mobile devices; 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; navigation, surveying, photographic, cinematographic, audio-visual, optical, weighing, life-saving and teaching apparatus and instruments; downloadable publications; downloadable and recorded media including written, image, video, audio and visual content, infographics, podcasts and webinars; downloadable educational materials; downloadable electronic educational materials; downloadable data sets; downloadable data sets relating to regulatory compliance in the medical and life sciences industries. Business management, organization and administration; office functions; collection, compilation, analysis, reporting and dissemination of statistics, data and information; 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, in the nature of administrative assistance, namely, assisting others in preparing and filing applications for regulatory approval of medical devices, medical technologies, medications, pharmaceuticals, and biotechnology; providing information online regarding regulatory submission management in the nature of administrative assistance; business and advisory consultancy services relating to obtaining and maintaining CE certifications. 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. Medical consultation; 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 CE 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. Scientific, technological and industrial analysis, research and design services; conducting and designing clinical trials; laboratory testing; consultancy services related to laboratory testing; clinical research; biological research, clinical 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; 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]; providing online, non-downloadable software; software design, development and engineering; computer software consultancy; providing online, non-downloadable 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 above mentioned services.

Class:

Legal services

Published for Opposition Date:

N/A

Mark Drawing Status:

4

Business Name:

N/A