QARALINK
LIVE

Serial Number

79419101

Owner

QARAlink SA

Attorney

Andrea L. Hintz

Filing Date

Oct 15, 2024

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QARALINK Trademark

Serial Number: 79419101 • Registration: 8237507

QARALINK is a trademark filed by QARAlink SA on October 15, 2024. The trademark is classified under Class 9 (Computers & Electronics), Class 38 (Telecommunications), Class 42 (Computer & Scientific), Class 35 (Advertising & Business). The application is currently registered and active.

Owner Contact Info

QARAlink SA

Route de la Pale 20

Entity Type: 98

Trademark Details

Filing Date

October 15, 2024

Registration Date

May 5, 2026

Published for Opposition

March 17, 2026

Goods & Services

Scientific and technological services, as well as research and design services relating thereto, namely, scientific consulting assistance for biological laboratory analytical testing to provide scientific information for regulatory compliance purposes; quality control for others and authentication services, namely, medical product and medical device authentication service; design and development of computers and software; development and testing of computing methods, algorithms and software, the aforesaid services not in connection with positioning systems and actuators, nor industrial valves, nor industrial automation, nor pumps or measuring or control systems for industrial installations; scientific and technological services and research and design relating thereto, namely, providing scientific research in the field of medical devices for regulatory compliance purposes; developing and testing computing methods, algorithms and software in the field of human health, medical devices and related regulatory affairs; scientific and technological services, namely, scientific research and computer programming in the field of artificial intelligence, not in relation to positioning systems and actuators, nor industrial valves, nor industrial automation, nor pumps or measuring or control systems for industrial installations; scientific and technological services, namely, scientific consulting assistance in the field of artificial intelligence in the field of human health, medical devices and related regulatory affairs; software as a service (SaaS) featuring software for regulatory assessment of medical devices and in vitro diagnostic devices, not in relation to positioning systems and actuators, nor industrial valves, nor industrial automation, nor pumps or measuring or control systems for industrial installations; software as a service (SaaS) featuring software for the collection and preparation of regulatory documentation in the field of human health; hosting an Internet platform; Platform as a Service (PaaS) featuring computer software platforms for conformity and regulatory assessment of medical products, medical devices and in vitro diagnostics; programming of software for information platforms on the Internet, these platforms not in relation to positioning systems and actuators, nor industrial valves, nor industrial automation, nor pumps or measuring or control systems for industrial installations; development of computer platforms in the field of regulatory file preparation, analysis and monitoring; design and development of computer hardware and software, namely in relation to the preparation of regulatory and marketing authorization files; testing, analysis and evaluation of third-party goods and services to determine conformity with certification standards; quality testing of products to determine conformity with certification standards; testing services to determine conformity with certification and quality control standards, the aforesaid testing services not in relation to positioning systems and actuators, nor industrial valves, nor industrial automation, nor pumps or measuring or control systems for industrial installations; scientific research services, namely, clinical trial data analysis and provision of scientific research information in the field of clinical trials for third parties

downloadable software for use in the preparation of regulatory documentation and regulatory authentication, excluding software for positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; downloadable database management software, excluding software for managing data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; downloadable software for searching data in the nature of search engine software, except for searching data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; downloadable data mining software for retrieving usable data from a wider set of raw data, except data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; downloadable software for determining and structuring the actions needed for the purposes of regulatory approval of medical devices; downloadable software for the segmentation of medical apparatus according to regulatory requirements; downloadable software for integrating regulatory data; downloadable software for integrating regulatory data in the field of medical devices; downloadable computer software in the fields of medicines and medical devices, pharmacy, pharmacology, pharmacovigilance, and clinical trials for generating manufacturing authorizations, certificates of good manufacturing practices, and lists of controlled terms and controlled vocabulary

Analysis and assessment of data in a central file, namely, computerized file management; compilation of information in computer databases except data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; compilation and data entry of information into computer databases, except data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling industrial installations; management of computer databases in the fields of medicines, medical devices, pharmacy, pharmacology, pharmacovigilance, clinical trials, manufacturing authorizations, certificates of good manufacturing practices, lists of controlled terms and controlled vocabulary

Providing access to computer databases, the aforesaid database data not in relation to positioning systems and actuators, nor to industrial valves, nor to industrial automation, nor to pumps or measuring or control systems for industrial installations; providing access to computer databases in the field of clinical trials and regulatory affairs; providing access to computer databases in the field of standards with respect to medical devices; providing access to a computer database and providing access time to a computer database, namely in the field of medicines, pharmacy, medical devices, pharmacology, pharmacovigilance, clinical trials, manufacturing authorizations, certificates of good manufacturing practices, lists of controlled terms and controlled vocabulary; Electronic exchange of data stored in databases accessible via telecommunication networks; transmission of database information via telecommunications networks, except data from positioning systems and actuators, industrial valves, industrial automation, pumps or systems for measuring or controlling installations

Filing History

NOTICE OF REGISTRATION CONFIRMATION EMAILED
May 5, 2026 NRCC
REGISTERED-PRINCIPAL REGISTER
May 5, 2026 R.PR
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
Mar 17, 2026 NPUB
PUBLISHED FOR OPPOSITION
Mar 17, 2026 PUBO
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
Mar 11, 2026 NONP
APPROVED FOR PUB - PRINCIPAL REGISTER
Feb 23, 2026 CNSA
TEAS/EMAIL CORRESPONDENCE ENTERED
Feb 4, 2026 TEME
CORRESPONDENCE RECEIVED IN LAW OFFICE
Feb 4, 2026 CRFA
TEAS REQUEST FOR RECONSIDERATION RECEIVED
Feb 4, 2026 ERFR
NOTIFICATION OF FINAL REFUSAL EMAILED
Jan 20, 2026 GNFN
FINAL REFUSAL E-MAILED
Jan 20, 2026 GNFR
FINAL REFUSAL WRITTEN
Jan 20, 2026 CNFR
TEAS/EMAIL CORRESPONDENCE ENTERED
Dec 3, 2025 TEME
CORRESPONDENCE RECEIVED IN LAW OFFICE
Dec 3, 2025 CRFA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
Dec 3, 2025 TROA
REFUSAL PROCESSED BY IB
Jun 28, 2025 RFNT
NON-FINAL ACTION MAILED - REFUSAL SENT TO IB
Jun 9, 2025 RFCS
REFUSAL PROCESSED BY MPU
Jun 9, 2025 RFRR
NON-FINAL ACTION (IB REFUSAL) PREPARED FOR REVIEW
Apr 6, 2025 RFCR
NON-FINAL ACTION WRITTEN
Apr 5, 2025 CNRT
ASSIGNED TO EXAMINER
Mar 24, 2025 DOCK
APPLICATION FILING RECEIPT MAILED
Mar 16, 2025 MAFR
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Mar 16, 2025 NWOS
SN ASSIGNED FOR SECT 66A APPL FROM IB
Mar 13, 2025 REPR