Trademark Overview
On Sunday, December 22, 2024, a trademark application was filed for CIMS ESYSTEM with the United States Patent and Trademark Office. The USPTO has given the CIMS ESYSTEM trademark a serial number of 79418991. The federal status of this trademark filing is NEW APPLICATION - RECORD INITIALIZED NOT ASSIGNED TO EXAMINER as of Thursday, March 13, 2025. This trademark is owned by CIMS eSystems A/S. The CIMS ESYSTEM trademark is filed in the Computer & Software Products & Electrical & Scientific Products and Computer & Software Services & Scientific Services categories with the following description:
Software and application software; software and application software, for use in document management within regulated industries, including the pharmaceutical and medical industries, the biotech industry, the life sciences industry and the medtech industry; software for the administration of clinical trials and research data; software to ensure compliance with relevant regulations and secure handling of data and documentation, including compliance with global pharmaceutical regulations; software with functionality for electronic signatures in accordance with global standards; software for simplifying and controlling the approval and documentation processes in regulated industries; quality management software that ensures compliance with industry and regulatory standards; clinical information management software to support regulatory compliance and quality management processes; software for managing technical files and master files related to product registration and compliance with leg...
Software as a service [SaaS]; Software as a service [SaaS] with software for use in document management within regulated industries, including the pharmaceutical and medical industries, the biotech industry, the life sciences industry and the medtech industry; Software as a service [SaaS] with software for managing clinical trials and research data; Software as a service [SaaS] with software to ensure compliance with relevant regulations and secure handling of data and documentation, including compliance with global pharmaceutical regulations; Software as a service [SaaS] with software with functionality for electronic signatures in accordance with global standards; Software as a service [SaaS] with software to simplify and control the approval and documentation processes in regulated industries; Software as a service [SaaS] with quality management software that ensures compliance with industry and regulatory standards; Software as a service [SaaS] with clinical information management ...
