TRIAL
Dead / Abandoned — Abandoned — failure to respond (as of 20 Feb 2024)
What this means for you
This application is over — abandoned 08 Feb 2024. The name may be available, but check before relying on it — rights can also come from actual use, not only from the register.
Record
- Serial number
- 79357620
- Mark type
- Design + words
- Filed
- 15 Sept 2022
- Abandoned
- 08 Feb 2024
Goods and services
- Class 009 — Scientific and electric apparatus: Software; software and applications for mobile devices; downloadable software applications; specialized software; collaborative software; data communication software; file sharing software; document management software; software for management of data and files and for databases; process control software; data processing software; product lifecycle management software; industrial process management software; software for production process monitoring, analysis, control and operation; software for verification of the regulatory compliance of goods; software for monitoring the regulatory compliance of clinical trials; software for quality control in the field of medical devices and the pharmaceutical industry; software for use in the pharmaceutical and medical device industry for monitoring, analysis, control and operation of the regulatory compliance of manufacturing processes and clinical trials
- Class 038 — Telecommunications services: Providing access to and rental of access time to a database; providing access to data or documents in electronic format on centralized files for remote consultation; providing access to platforms and portals on the Internet; electronic transmission of messages, data and documents
- Class 042 — Scientific and technological services: Hosting services and software as a service and rental of software; development, programming and implementation of software; development, programming and implementation of data processing software; development, programming and implementation of software for checking the regulatory compliance of goods; development, programming and implementation of software for quality control of goods and clinical studies; accreditation services (certification of skills and quality) in the field of medical devices and the pharmaceutical industry; certification (quality control); quality control consultation; analysis and assessment of product design in the field of medical devices and the pharmaceutical industry; qualitative assessment of the performance of pharmaceuticals, medical products and medical devices; providing information on product development; preliminary assessment services in the field of new pharmaceuticals, medical products and medical devices; pharmaceutical research and development consultation services; consultation services on product development in the field of medical devices and the pharmaceutical industry; providing information on the results of clinical trials for pharmaceuticals, medical products and medical devices; design and development of medical technologies; design and development of analytical methods and tests; research and development services in the field of medical devices and pharmaceuticals; scientific and technological design services; conducting of scientific feasibility studies; carrying out technical feasibility studies; feasibility studies with respect to product design; feasibility studies with respect to analysis of materials; feasibility studies with respect to clinical trials; planning and conducting preclinical and clinical studies; providing medical and scientific research information of pharmaceuticals and clinical trials; conducting clinical trials for third parties (scientific research); conducting clinical trials for pharmaceuticals, medical products and medical apparatus; conducting of clinical studies; scientific research; medical research; pharmaceutical research and development; study of technical projects in the field of medical devices and the pharmaceutical industry; assessment of chemical information in relation to risks; assessment of toxicological information in relation to risks; risk assessment in the field of medical devices and the pharmaceutical industry; scientific assessment of risks; analytical laboratory services; laboratory research services relating to pharmaceuticals, medical devices and medical products; scientific laboratory services; advisory services with respect to laboratory tests; scientific diagnostic test services
Owner
- 1MED SA, CH
Prosecution history
- 03 Oct 2025 — NEW REPRESENTATIVE AT IB RECEIVED
- 15 Mar 2025 — FINAL DECISION TRANSACTION PROCESSED BY IB
- 21 Feb 2025 — FINAL DISPOSITION NOTICE SENT TO IB
- 21 Feb 2025 — FINAL DISPOSITION NOTICE CREATED, TO BE SENT TO IB
- 11 Jun 2024 — NOTIFICATION OF POSSIBLE OPPOSITION - PROCESSED BY IB
- 15 May 2024 — NOTIFICATION OF POSSIBLE OPPOSITION SENT TO IB
- 15 May 2024 — NOTIFICATION OF POSSIBLE OPPOSITION CREATED, TO BE SENT TO IB
- 20 Feb 2024 — ABANDONMENT NOTICE MAILED - FAILURE TO RESPOND
- 20 Feb 2024 — ABANDONMENT NOTICE MAILED - FAILURE TO RESPOND
- 20 Feb 2024 — ABANDONMENT - FAILURE TO RESPOND OR LATE RESPONSE
- 29 Aug 2023 — REFUSAL PROCESSED BY IB
- 07 Aug 2023 — NON-FINAL ACTION MAILED - REFUSAL SENT TO IB
- 07 Aug 2023 — REFUSAL PROCESSED BY MPU
- 01 Jul 2023 — NEW REPRESENTATIVE AT IB RECEIVED
- 01 Jul 2023 — NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW