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The Union trademark AGOS was filed as Word mark on 11/19/2019 at the European Union Intellectual Property Office.
It was registered as a trademark on 02/25/2021.
The current status of the mark is "Trademark registered".
| Trademark form | Word mark |
| File reference | 018155143 |
| Application date | November 19, 2019 |
| Publication date | November 18, 2020 |
| Entry date | February 25, 2021 |
| Expiration date | November 19, 2029 |
Trademark owner
The Lawns, High Street, Offley
SG5 3AN Hitchin
GB
SG5 3AN Hitchin
GB
goods and services
9
Computer software in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; downloadable software applications in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; software for secure data storage and retrieval and transmission of customer and client information; computer software and computer programs and application development software for use on or in connection with mobile phones, tablets and handheld devices in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; data processing equipment and computers; electronic publications (downloadable) provided on-line from a database or the internet
35
Business management services; business consultancy services; business management and consultancy services in the field of clinical trials and clinical research; providing business intelligence services in the fields of medical devices, pharmaceuticals and the life sciences; providing business management information in connection with consultancy and advisory services in the field of strategic planning; business administration services in the field of regulatory submission management in the fields of new medical devices and new pharmaceuticals namely the provision of strategic planning, writing of documentation and submission of applications to the relevant regulatory authorities concerning medical devices, medicinal products, applications for clinical trial approval, marketing authorisation approval and related variations, requests for scientific advice, requests for SME status classification, requests for PRIME and other procedural processes, applications for orphan designation and applications for CE mark approval; assisting others in preparing and filing applications for new drugs with governmental regulatory bodies; pharmaceutical and biotechnology product commercialization; consultancy services for others in the field of pharmaceutical and biotechnology product commercialization; information, advice and consultancy services in relation to all the aforesaid services
38
Providing access to platforms and portals on the internet in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; providing user access to platforms and portals on the internet in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; information, advice and consultancy services in relation to all the aforesaid services
42
Providing medical and scientific research information in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; research and development in the field of pharmaceuticals, clinical trials, clinical research, medical devices and biotechnology; consultancy services for others in the field of pharmaceuticals, clinical trials, clinical research, medical devices and biotechnology; conducting early evaluations in the field of new pharmaceuticals; consultancy services in the field of design, planning, implementation and project management of clinical trials, pharmacovigilance, pharmaceutical and biotechnology product development; consultancy services in the fields of biotechnology, pharmaceutical research and development, laboratory testing and pharmacogenetics; medical and scientific research; conducting clinical trials for others; pharmaceutical drug development services; development of pharmaceutical preparations and medicines; pharmaceutical product evaluation; pharmaceutical research and development; product development consultancy in the field of pharmaceuticals and biotechnology; testing and quality control of products in the field of pharmaceuticals, clinical trials and biotechnology; testing and quality control of pharmaceutical preparations and medicines; testing and quality control of clinical trials in the field of pharmaceuticals and biotechnology; provision of clinical data and regulatory submission management services for medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; providing information management services on clinical trials and clinical research; Software as a Service [SaaS] in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; website and media content management services featuring non-downloadable software applications for use in creating, designing, hosting, publishing, managing and maintaining content for use on the internet; application service provider featuring application programming interface (API) software to allow people to view data through an interactive map, to query data, to generate reports and to access data and documents; software as a service (SAAS) featuring computer software to enable the displaying, receiving and transmitting of data to enable the purchase of goods and services; information, advice and consultancy services in relation to all the aforesaid services
44
Managed healthcare services in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; consultancy services in the field of medical information services; consultancy services in the field of pharmaceuticals, clinical trials, clinical research and biotechnology; consultancy services in the field of biotechnology diagnostics and pharmacogenetics diagnostics; information, advice and consultancy services in the pharmaceutical and healthcare sectors; information, advice and consultancy services in relation to pharmacovigilance; information, advice and consultancy services in relation to all the aforesaid services
45
Reviewing standards and practices to assure compliance with laws and regulations in the field of regulatory submission management in the fields of new medical devices and new pharmaceuticals namely the provision of strategic planning, writing of documentation and submission of applications to the relevant regulatory authorities concerning medical devices, medicinal products, applications for clinical trial approval, marketing authorisation approval and related variations, requests for scientific advice, requests for SME status classification, requests for PRIME and other procedural processes, applications for orphan designation and applications for CE mark approval
Trademark history
| Date | Document number | Area | Entry |
|---|---|---|---|
| March 16, 2021 | RAW: Representative - Deletion of the representative, Published |
ID: 11018155143