NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
05/21/2024
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Official data from USPTO
A
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Active USPTO registrationType: CombinedOffice: United States
Risk and opportunity diagnosis
Executive reading for naming, filing, and monitoring decisions.
USPTO status
Active USPTO registration
Case type
Application and registration
Recorded events
14
Latest update
05/21/2024
Trademark type
Combined
Nice classes
35, 42, 45
Filing date
05/01/2023
Registration date
05/21/2024
Expiration date
-
Complete case details
Structured fields from the responsible authority and the official record.
Status date
05/21/2024
Last transaction
05/21/2024
Responsible office
United States Patent and Trademark Office
Status code
700
Official register
Principal Register
First use anywhere
10/31/2022
First use in commerce
10/31/2022
Drawing code
3
Owner type
16
Owner location
Lake Mary, FL, US
Examiner
PHILLIPS, WENDELL
Law office
M10
Current location
FILE REPOSITORY (FRANCONIA)
Mark description
The mark consists of a stylized "A" comprised of four curved triangles.
Holders and representatives
Holders
Clinical Research Holdings, LLC
Representatives
Mark A. Wright McLane Middleton, P.A.
Technical classification
Nice Classes
Class 35Class 42Class 45
Vienna Codes
No Vienna codes available.
Goods and services
Class 35
Business consulting and management in the field of clinical trials in all phases as it relates to pre-study document collection and reviewsite selectionvisits and auditssite complianceproject tracking and monitoring reportsnegotiation and administration of investigator grants and clinical trial budgets and contractsfinancial and management accountingdistributioncoordination and tracking of clinical trial products and materialsregulatory document processinglaboratory 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 protocolscontractsbudgetsamendmentspaper and electronic case report formsinformed consent formssafety narrativespresentation posterstraining manuals; Business consulting and management in the field of clinical trials in all phases as it relates to managing all aspects of studydrug reconciliationinventory and distribution reports; Business management for all aspects of clinical trials in all phases as it relates to managing investigatorscoordinatorsmonitorstechniciansparticipants 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 reviewssubmitting clinical trial protocols to institutional review boards and independent ethics committees on behalf of medicalbiopharmaceutical 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 managementmanaging randomization logisticsin the pharmaceutical and biotechnological field for business purposes; Development and implementation of personnel recruitment and retention programs for investigatorscoordinatorsmonitorstechnicians 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 medicalpharmaceutical and biotechnological field for business purposes
Class 42
Medical and scientific research consulting services for others in the field of designplanningimplementation of clinical trials in all phases; providing quality assurance services in the pharmaceutical and biotechnological industries
Class 45
Regulatory affairsreviewing standards and practices to assure compliance with clinical trial laws and regulations; Providing independent review of clinical trials involving human subjectsreviewing research protocols and related information to ensure protection of the rights and welfare of human subjects of research
Publications
History of USPTO decisions and trademark events.
14 publications found
R.PR
REGISTERED-PRINCIPAL REGISTER
05/21/2024
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
03/05/2024
PUBO
PUBLISHED FOR OPPOSITION
03/05/2024
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
02/14/2024
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
02/14/2024
TCCA
TEAS CHANGE OF CORRESPONDENCE RECEIVED
01/29/2024
ARAA
ATTORNEY/DOM.REP.REVOKED AND/OR APPOINTED
01/29/2024
REAP
TEAS REVOKE/APP/CHANGE ADDR OF ATTY/DOM REP RECEIVED
01/29/2024
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
01/26/2024
DOCK
ASSIGNED TO EXAMINER
01/26/2024
MDSM
NOTICE OF DESIGN SEARCH CODE E-MAILED
05/31/2023
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
05/30/2023
NWAP
NEW APPLICATION ENTERED
05/04/2023
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