REGISTERED
on 21 May 2024
Last Applicant/ Owned by
615 Crescent Executive Ct, Suite 120
Lake Mary
FL
32746
Serial Number
97915043 filed on 01st May 2023
Registration Number
7391557 registered on 21st May 2024
Correspondent Address
Mark A. Wright McLane Middleton, P.A.
Filing Basis
1. filed as use application
2. use application currently
Disclaimer
NO DATA
A
Medical and scientific research consulting services for others in the field of design, planning, and implementation of clinical trials in all phases; providing quality assurance services in the pharmaceutical and biotechnological industries Regulatory affairs, namely, reviewing standards and practices to assure compliance with clinical trial laws and regulations; Providing independent review of c Read More
Classification Information
Class [045]
Personal & Legal & Social Services
Regulatory affairs, namely, reviewing standards and practices to assure compliance with clinical trial laws and regulations; 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
First Use Date in General
31st Oct 2022
First Use Date in Commerce
31st Oct 2022
Class [042]
Computer & Software Services & Scientific Services
Medical and scientific research consulting services for others in the field of design, planning, and implementation of clinical trials in all phases; providing quality assurance services in the pharmaceutical and biotechnological industries
First Use Date in General
31st Oct 2022
First Use Date in Commerce
31st Oct 2022
Class [035]
Advertising, Business & Retail Services
Business consulting and management in the field of clinical trials in all phases as it relates to pre-study document collection and review, site selection, visits and audits, site compliance, project tracking and monitoring reports, negotiation and administration of investigator grants and clinical trial budgets and contracts, financial and management accounting, distribution, coordination and tracking of clinical trial products and materials, regulatory document processing, laboratory selection and coordination; Business consulting and management in the field of clinical trials in all phases as it relates to managing site and study-specific subject recruitment strategies and programs in the nature of contingency strategies and solutions to address specific project challenges; Business consulting and management in the field of clinical trials in all phases as it relates to managing the development of all study related documents and materials in the nature of study protocols, contracts, budgets, amendments, paper and electronic case report forms, informed consent forms, safety narratives, presentation posters, and training manuals; Business consulting and management in the field of clinical trials in all phases as it relates to managing all aspects of study, drug reconciliation, and inventory and distribution reports; Business management for all aspects of clinical trials in all phases as it relates to managing investigators, coordinators, monitors, technicians, and participants for compliance with clinical protocols and regulations; Business consulting and management in the field of clinical trials in all phases as it relates to management and compilation of computerized databases in the field of clinical trials for business purposes; Business consulting and management in the field of clinical trials in all phases as it relates to ethical reviews, namely, submitting clinical trial protocols to institutional review boards and independent ethics committees on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical trials; Statistical analysis and reporting services for business purposes in the field of clinical trials; Business project management in the field of clinical trials in all phases as it relates to organizing and conducting business meetings of clinical trial investigators; Business management, namely, managing randomization logistics, in the pharmaceutical and biotechnological field for business purposes; Development and implementation of personnel recruitment and retention programs for investigators, coordinators, monitors, technicians and participants for use in clinical trials; Business consulting and management in the field of clinical trials in all phases as it relates to the administration of protocols involving volunteer research patients and the recruiting of such volunteer research patients; Providing data management services in the medical, pharmaceutical and biotechnological field for business purposes
First Use Date in General
31st Oct 2022
First Use Date in Commerce
31st Oct 2022
Mark Details
Serial Number
No 97915043
Mark Type
No Service Mark
Attorney Docket Number
No 128777
44D Filed
No
44D Current
No
44E filed
No
44E Current
No
66A Filed
No
66A Current
No
Current Basis
No
No Basis
No
Design Code(s)
26.05.15 -
Four or more triangles
26.05.21 -
Triangles that are completely or partially shaded
26.05.25 -
Triangles with one or more curved sides
27.03.01 -
Geometric figures forming letters or numerals, including punctuation
Description of Design Search
The mark consists of a stylized "A" comprised of four curved triangles.
Legal History
| Status Date | Action Taken |
|---|---|
| 21st May 2024 | NOTICE OF REGISTRATION CONFIRMATION EMAILED |
| 21st May 2024 | REGISTERED-PRINCIPAL REGISTER |
| 05th Mar 2024 | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED |
| 05th Mar 2024 | PUBLISHED FOR OPPOSITION |
| 14th Feb 2024 | NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED |
| 14th Feb 2024 | OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED |
| 29th Jan 2024 | TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED |
| 29th Jan 2024 | ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED |
| 29th Jan 2024 | TEAS CHANGE OF CORRESPONDENCE RECEIVED |
| 26th Jan 2024 | APPROVED FOR PUB - PRINCIPAL REGISTER |