ADVANCING CLINICAL RESEARCH: SAFER, SMARTER, FASTER Trademark

Trademark Overview


On Wednesday, October 13, 2021, a trademark application was filed for ADVANCING CLINICAL RESEARCH: SAFER, SMARTER, FASTER with the United States Patent and Trademark Office. The USPTO has given the ADVANCING CLINICAL RESEARCH: SAFER, SMARTER, FASTER trademark a serial number of 97072496. The federal status of this trademark filing is REGISTERED as of Tuesday, November 29, 2022. This trademark is owned by Advarra, Inc.. The ADVANCING CLINICAL RESEARCH: SAFER, SMARTER, FASTER trademark is filed in the Advertising, Business and Retail Services, Insurance & Financial Services, Education & Entertainment Services, Computer & Software Services & Scientific Services, Personal, and Legal & Social Services categories with the following description:

Providing online education, namely, providing online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable electronic publications in the nature of articles, blog posts, case studies, and e-learning modules in the field of clinical, medical, and biological research studies; developing, arranging and conducting business conferences in the field of clinical, medical, and biological research studies

Financial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare

Business consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered...

Providing regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects; providing institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices...

Providing information in the field of medical and scientific research on the internet; providing digital content, namely, e-learning solutions in the nature of software as a service (SAAS) services featuring software for database management and information management relating to clinical trials, on the internet; providing temporary use of on-line non-downloadable software for use by clinical, medical, and biological researchers, research sponsors and clinical research organizations for use in automating the submission, review and approval process of human subject clinical research projects and providing access to forms and templates to researchers, research sponsors and clinical research organizations for automating the submission, review and approval of human subject clinical research projects; providing temporary use of non-downloadable computer software for use in healthcare and research for the management and administration of research for the protection of research participants by...
advancing clinical research: safer, smarter, faster

General Information


Serial Number97072496
Word MarkADVANCING CLINICAL RESEARCH: SAFER, SMARTER, FASTER
Filing DateWednesday, October 13, 2021
Status700 - REGISTERED
Status DateTuesday, November 29, 2022
Registration Number6910770
Registration DateTuesday, November 29, 2022
Mark Drawing4000 - Illustration: Drawing with word(s) / letter(s) / number(s) in Block form
Published for Opposition DateTuesday, September 13, 2022

Trademark Statements


Goods and ServicesProviding online education, namely, providing online courses of instruction from a computer database or via the internet or extranet in the fields of clinical trials; developing, arranging, and conducting educational conferences in the field of clinical, medical, and biological research studies; educational services, namely, providing online, non-downloadable webinars, seminars, and conferences in the field of clinical, medical, and biological research studies; non-downloadable electronic publications in the nature of articles, blog posts, case studies, and e-learning modules in the field of clinical, medical, and biological research studies; developing, arranging and conducting business conferences in the field of clinical, medical, and biological research studies
Goods and ServicesFinancial advisory services, namely, budget negotiation and budget set-up services in the field of clinical trials involving human subjects; insurance coverage consultancy services, namely, determining whether particular goods and services in clinical trials are covered by Medicare
Goods and ServicesBusiness consulting; business administrative assistance, namely, business support services for the preparation and filing of institutional biosafety committee and institutional review board forms for use in the field of human subject research; business management consultation services concerning organization transformation in the field of clinical trials involving human subjects; professional staffing services in the field of medical and scientific research; organizing and administering a network of research sites, namely, business consultation and management in the field of clinical trials, specifically, providing governmental registration assistance in the nature of regulatory submission management on behalf of research sites that conduct gene therapy and vaccine research to assist them with clinical research and clinical trials; providing institutional biosafety committee services, namely, providing independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research for business purposes
Goods and ServicesProviding regulatory compliance consultation services in the nature of advice concerning due diligence, strategic development, and regulatory policy in the field of clinical trials involving human subjects; providing independent review of clinical trials involving human subjects, namely, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; providing information relating to regulatory compliance for independent review of clinical trials involving human subjects; providing institutional biosafety committee services, namely, independent review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, reviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, reviewing standards and practices to assure compliance with laws and regulations in the field of clinical trials involving human subjects; regulatory compliance consultation services in the nature of health inspection readiness and remediation in the field of clinical, medical, and biological research studies; consultation services in the field of pharmacovigilance strategies to ensure regulatory compliance and patient safety in the field of clinical trials involving human subjects; regulatory compliance consultation services in the field of informed consent protocols for clinical trial participants; consultation services in the field of research compliance, namely, regulatory compliance consultation services in the field of clinical trials involving human subjects
Goods and ServicesProviding information in the field of medical and scientific research on the internet; providing digital content, namely, e-learning solutions in the nature of software as a service (SAAS) services featuring software for database management and information management relating to clinical trials, on the internet; providing temporary use of on-line non-downloadable software for use by clinical, medical, and biological researchers, research sponsors and clinical research organizations for use in automating the submission, review and approval process of human subject clinical research projects and providing access to forms and templates to researchers, research sponsors and clinical research organizations for automating the submission, review and approval of human subject clinical research projects; providing temporary use of non-downloadable computer software for use in healthcare and research for the management and administration of research for the protection of research participants by automating the conduct of research studies and consent of research participants; providing institutional biosafety committee services, namely, review and oversight of clinical trials involving genetically engineered gene therapy and vaccine research, specifically, evaluating research sites involved in gene therapy and vaccine research clinical trials to determine whether the organizations conform to an established accreditation standard; assessing the readiness of research sites to conduct gene therapy and vaccine research, namely, testing, analysis, and evaluation of gene therapy and vaccine research service providers to determine conformity with established accreditation standards; consultation services in the nature of quality management, namely, quality evaluation and analysis, quality assurance, and quality control in the field of clinical, medical, and biological research studies; consultation services in the field of drug and medical device development; consultation services in the field of conducting clinical trials for others; consultation services in the field of scientific research compliance, namely, analysis and evaluation of scientific research of others in the field of clinical trials involving human subjects to assure compliance with industry standards; consultation services in the field of scientific research administration and operations in the field of clinical trials involving human subjects; consultation services in the field of product research and development and scientific research and development; consulting services in the field of medical and scientific research for clinical trials; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for use in the design, administration, and tracking of clinical, medical, and biological research studies; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in the storage, analysis, and transfer of data related to clinical, medical, and biological research studies; providing online non-downloadable software for use in collecting and managing consents from participants in clinical, medical, and biological research studies; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in regulatory reporting, compliance tracking, safety monitoring, and evaluation of clinical, medical, and biological research studies; providing online non-downloadable software enabling real-time communication for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, and institutional review boards in clinical, medical, and biological research studies; providing online non-downloadable software for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff in managing stipends and travel reimbursements in clinical, medical, and biological research studies; providing online non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, and contract research organizations in the design and administration of scientific and medical research projects and of clinical trials for pharmaceuticals, medical devices and medical procedures; providing online non-downloadable software for use by pharmaceutical companies and clinical, medical, and biological research study sponsors, contract research organizations, research sites, and research site staff for data collection, data sharing, information exchange, and collaboration regarding scientific and medical research projects and regarding clinical trials for pharmaceuticals, medical devices and medical procedures; providing online non-downloadable software in the nature of a support platform for use by clinical, medical, and biological research study sponsors, contract research organizations, research sites, research site staff, study teams and patients for use in information management in the performance of a clinical trial; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by academic medical centers and cancer centers; providing online non-downloadable software in the nature of a clinical trial management system for data processing and information management for use by clinical, medical, and biological research sites, site networks, hospitals, and health systems; providing online non-downloadable teaching software system in the nature of an e-learning apparatus support platform for content delivery, patient recruitment management, and learning process management and reporting for use by clinical, medical, and biological research site staff, study teams and patients relating to clinical trials; providing online non-downloadable software for patient identification for use by clinical, medical, and biological researchers for patients enrolled in clinical trials; providing online non-downloadable software for patient scheduling and tracking for use by clinical, medical, and biological research sites and patients enrolled in clinical trials; troubleshooting of computer software problems; providing temporary use of non-downloadable cloud-based software for transmitting clinical trial data; business technology software consultation services regarding the implementation of computer software provided online for use in healthcare and research that is for the management and administration of research, the protection of research participants, and the automation and facilitation of the conduct of research studies and electronic consent of research participants; providing online education, namely, software as a service (SAAS) services featuring e-learning software for providing online courses of instruction relating to clinical trials in the field of medicine

Classification Information


International Class035 - Advertising; business management; business administration; office functions.
US Class Codes100, 101, 102
Class Status Code6 - Active
Class Status DateTuesday, August 9, 2022
Primary Code035
First Use Anywhere DateTuesday, August 10, 2021
First Use In Commerce DateTuesday, August 10, 2021

International Class036 - Insurance; financial affairs; monetary affairs; real estate affairs.
US Class Codes100, 101, 102
Class Status Code6 - Active
Class Status DateWednesday, November 3, 2021
Primary Code036
First Use Anywhere DateTuesday, August 10, 2021
First Use In Commerce DateTuesday, August 10, 2021

International Class041 - Education; providing of training; entertainment; sporting and cultural activities.
US Class Codes100, 101, 107
Class Status Code6 - Active
Class Status DateWednesday, November 3, 2021
Primary Code041
First Use Anywhere DateTuesday, August 10, 2021
First Use In Commerce DateTuesday, August 10, 2021

International Class042 - Scientific and technological services and research and design relating thereto; industrial analysis and research services; design and development of computer hardware and software.
US Class Codes100, 101
Class Status Code6 - Active
Class Status DateTuesday, August 9, 2022
Primary Code042
First Use Anywhere DateTuesday, August 10, 2021
First Use In Commerce DateTuesday, August 10, 2021

International Class045 - Legal services; security services for the protection of property and individuals; personal and social services rendered by others to meet the needs of individuals.
US Class Codes100, 101
Class Status Code6 - Active
Class Status DateTuesday, August 9, 2022
Primary Code045
First Use Anywhere DateTuesday, August 10, 2021
First Use In Commerce DateTuesday, August 10, 2021

Trademark Owner History


Party NameAdvarra, Inc.
Party Type30 - Original Registrant
Legal Entity Type03 - Corporation
AddressColumbia, MD 21044

Party NameAdvarra, Inc.
Party Type20 - Owner at Publication
Legal Entity Type03 - Corporation
AddressColumbia, MD 21044

Party NameAdvarra, Inc.
Party Type10 - Original Applicant
Legal Entity Type03 - Corporation
AddressColumbia, MD 21044

Trademark Events


Event DateEvent Description
Wednesday, January 25, 2023ASSIGNMENT OF OWNERSHIP NOT UPDATED AUTOMATICALLY
Tuesday, November 29, 2022NOTICE OF REGISTRATION CONFIRMATION EMAILED
Tuesday, November 29, 2022REGISTERED-PRINCIPAL REGISTER
Wednesday, November 2, 2022ASSIGNMENT OF OWNERSHIP NOT UPDATED AUTOMATICALLY
Tuesday, September 13, 2022OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
Tuesday, September 13, 2022PUBLISHED FOR OPPOSITION
Wednesday, August 24, 2022NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
Tuesday, August 9, 2022APPROVED FOR PUB - PRINCIPAL REGISTER
Tuesday, August 9, 2022EXAMINER'S AMENDMENT ENTERED
Tuesday, August 9, 2022NOTIFICATION OF EXAMINERS AMENDMENT E-MAILED
Tuesday, August 9, 2022EXAMINERS AMENDMENT E-MAILED
Tuesday, August 9, 2022EXAMINERS AMENDMENT -WRITTEN
Friday, July 29, 2022TEAS/EMAIL CORRESPONDENCE ENTERED
Thursday, July 28, 2022CORRESPONDENCE RECEIVED IN LAW OFFICE
Thursday, July 28, 2022TEAS RESPONSE TO OFFICE ACTION RECEIVED
Monday, February 14, 2022NOTIFICATION OF NON-FINAL ACTION E-MAILED
Monday, February 14, 2022NON-FINAL ACTION E-MAILED
Monday, February 14, 2022NON-FINAL ACTION WRITTEN
Thursday, December 23, 2021ASSIGNED TO EXAMINER
Wednesday, November 3, 2021NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Saturday, October 16, 2021NEW APPLICATION ENTERED