CIMS ESYSTEM

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 legal requirements, in relation to the medical, pharmaceutical and biotechnology field.

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 software to support regulatory compliance and quality management processes; Software as a service services [SaaS] with software for managing technical files and master files related to product registration and regulatory compliance relating to the medical field and in the pharmaceutical field, Biotechnology, and life sciences and medical technology; adaptation of software for integration into existing IT infrastructures that increase flexibility and efficiency in handling regulatory information in relation to the medical field, in the pharmaceutical field, Biotechnology, and life sciences, Medical technology; consulting services, including in relation to design and customization of computer software for document and quality management systems tailored to the specific needs of the pharmaceutical, medical, biotech, life science and medtech industries.