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Application Number:8061880
Status:
Ready for Examination
Class:42
Filing Date:Wed, 14 Oct 2026

Trademark Information

TrademarkEASYQ
Trademark TypeWordmark
Class42
Application Number8061880
Nature/Scope of businessSoftware as a service [SaaS]; platform as a service [PaaS]; software as a service [SaaS] and platform as a service [PaaS] featuring cloud-based, artificial intelligence (AI)-enabled electronic quality management system (eQMS) software; providing online non-downloadable computer software for quality management, regulatory compliance and lifecycle management of medical devices, in vitro diagnostic devices, software as a medical device (SaMD) and healthcare technologies; providing online non-downloadable computer software for document management, risk management, corrective and preventive action (CAPA) management, training management, complaint management, management review, audit management, change control, supplier management, design control, design history file management, requirements traceability and regulatory compliance management; providing online non-downloadable computer software for creating, managing, maintaining, storing and retrieving electronic records and electronic signatures; providing online non-downloadable computer software for conducting gap assessments, compliance assessments and evaluations against applicable quality management and regulatory standards; providing virtual computer systems through cloud computing; electronic data storage; off-site data backup; server hosting; design and development of computer software; installation of computer software; maintenance of computer software; updating of computer software; customization of computer software; information technology [IT] support services [troubleshooting of software]; computer software consultancy; conversion of computer programs and data, other than physical conversion; data security consultancy; quality control; quality control of computer software and computerised systems, namely computer system validation and software verification and validation testing for software used in regulated healthcare environments and software as a medical device (SaMD); technological consultancy; technological consultancy relating to quality management systems, medical device design controls and software lifecycle management; technical writing; technical writing, namely preparation of technical documentation, technical files, design history files, risk management files and clinical evaluation reports for medical devices and healthcare technologies; technological research; research and development of new products for others; clinical trials; medical research; all included in Class 42
Status
Ready for Examination
Applicant: EASYQ SOLUTIONS AND TECHNOLOGIES PRIVATE LIMITED
Applicant Address1092, SOBHA MOONSTONE, DASARAHALLI MAIN ROAD, HEBBAL, BENGALURU, BENGALURU URBAN, KARNATAKA 560024
JurisdictionCHENNAI
AgentAAKASH RAMAN SINHA[35430]
Agent Address002, Sai Pushpa Apartment, Davis Road, Cooke Town, Bengaluru - 560 005

Frequently Asked Questions

What is the status of trademark EASYQ? ▾
The trademark application number 8061880 is currently marked as "Ready for Examination" in the official trademark registry.
Who is the owner of trademark EASYQ? ▾
The trademark application number 8061880 is owned by EASYQ SOLUTIONS AND TECHNOLOGIES PRIVATE LIMITED.
Which class does trademark EASYQ belong to? ▾
Trademark application number 8061880 is filed under Class 42, which relates to the specified goods and services.
Who is the trademark agent for application 8061880? ▾
The trademark agent associated with application number 8061880 is AAKASH RAMAN SINHA[35430].
What is trademark EASYQ? ▾
Trademark application number 8061880 relates to "Software as a service [SaaS]; platform as a service [PaaS]; software as a service [SaaS] and platform as a service [PaaS] featuring cloud-based, artificial intelligence (AI)-enabled electronic quality management system (eQMS) software; providing online non-downloadable computer software for quality management, regulatory compliance and lifecycle management of medical devices, in vitro diagnostic devices, software as a medical device (SaMD) and healthcare technologies; providing online non-downloadable computer software for document management, risk management, corrective and preventive action (CAPA) management, training management, complaint management, management review, audit management, change control, supplier management, design control, design history file management, requirements traceability and regulatory compliance management; providing online non-downloadable computer software for creating, managing, maintaining, storing and retrieving electronic records and electronic signatures; providing online non-downloadable computer software for conducting gap assessments, compliance assessments and evaluations against applicable quality management and regulatory standards; providing virtual computer systems through cloud computing; electronic data storage; off-site data backup; server hosting; design and development of computer software; installation of computer software; maintenance of computer software; updating of computer software; customization of computer software; information technology [IT] support services [troubleshooting of software]; computer software consultancy; conversion of computer programs and data, other than physical conversion; data security consultancy; quality control; quality control of computer software and computerised systems, namely computer system validation and software verification and validation testing for software used in regulated healthcare environments and software as a medical device (SaMD); technological consultancy; technological consultancy relating to quality management systems, medical device design controls and software lifecycle management; technical writing; technical writing, namely preparation of technical documentation, technical files, design history files, risk management files and clinical evaluation reports for medical devices and healthcare technologies; technological research; research and development of new products for others; clinical trials; medical research; all included in Class 42".

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