Serial #90027024
LIVE

Serial Number

90027024

Owner

US Data Management, LLC

Attorney

Darren B. Cohen

First Use Date

Nov 5, 2013

Filing Date

Jun 29, 2020

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Serial #90027024 Trademark

Serial Number: 90027024 • Registration: 6775548

Serial #90027024 is a trademark filed by US Data Management, LLC on June 29, 2020. The trademark is classified under Class 41 (Education & Entertainment), Class 42 (Computer & Scientific), Class 45 (Legal & Security Services), Class 35 (Advertising & Business). The application is currently registered and active.

Owner Contact Info

US Data Management, LLC (14 trademarks)

535 Chapala Street
Santa Barbara, CA 93101

Entity Type: 16

Trademark Details

Filing Date

June 29, 2020

Registration Date

June 28, 2022

First Use Anywhere

November 5, 2013

First Use in Commerce

November 5, 2013

Published for Opposition

August 3, 2021

Goods & Services

Providing educational programs in the life science fields using on-line activities, non-downloadable webinars and blogs, workshops, and printable materials distributed therewith featuring Regulatory issues and developments, GxP (Good Practice) Compliance, Risk Management, Design Control, QMS (Quality Management Solutions), CSV (Computer System Validation), SOP (Standard Operating Procedures), Data Integrity, UDI (Unique Device Identification), Regulatory readiness, and other related practice areas in the life sciences fields

Business advisory, development, and strategic planning services provided to companies for business purposes in the life sciences industries; Business consultation services in the field of GxP (Good Practice) compliance; Business consulting services on processes and workflows related to content creation, localization and publishing strategy including Translation Memory and Terminology Management, Quality Management, Life Sciences Regulatory Compliance and Risk Management; Business consulting and management in the field of clinical trials, namely, clinical data and regulatory submission management on behalf of medical, biopharmaceutical and biotechnology companies to assist them with clinical research, clinical trials and applications for drug approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology with governmental regulatory bodies around the world; Regulatory submission management, namely, providing simultaneous multiple country submissions of applications for the registration and approval of medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; providing information online regarding regulatory submission management; Business management consulting, strategic planning and business advisory services provided to medical, medical technology, biopharmaceutical, and biotechnology companies, and government agencies, educational and research institutions, law firms, and investment firms in the fields of biologics, pharmaceuticals and medical devices; Providing consulting services in the field of regulatory submission management to medical companies to assist them with applications for drug and medical device approval; Regulatory submission management, namely, assisting others in preparing and filing applications for new drugs and medical devices with governmental regulatory bodies; Business consulting services in the field of biologics, pharmaceuticals, prescription drugs and medical devices; Business consulting and management for companies in the life sciences fields pertaining to business operations including standard operating procedures, audits and assessments; Business consulting and for companies in the life sciences fields related to supply chain management, including, internet of medical things (IoMT), connected service and quality management, product lifecycle management, product master management, and enterprise resource planning; Providing quality and IT staffing services for companies in the life sciences fields and employment consultation pertaining to staffing augmentation services and onsite and remote on-demand compliance staff augmentation; Business consulting and management for companies in the life sciences fields pertaining to business operations including information and data compiling and analyzing relating to business management; consulting services in the field of medical device product approval for commercial purposes; Business consulting and management for companies in the life sciences fields for use in the following applications: validation and qualification; including, computer software assurance, manufacturing system validation, laboratory equipment and instrumentation, process validation and cleaning validation, laboratory information management systems (LIMS), facilities and utilities, and manufacturing systems; Business consulting and management for companies in the life sciences fields for use in the following applications: compliance strategy: including laboratory validation, assessments, strategy and remediation planning, performing remediation activities, and providing advisory services to assist GxP labs in meeting commercial and regulatory requirements; Business consulting and management for companies in the life sciences fields for use in the following applications: digital transformation strategy, including: support on demand services, development on demand services; Business consulting and management for companies in the life sciences fields for use in the following applications: management; including life sciences and program management, GxP cloud services, and organizational change management

Regulatory compliance consulting services in the life sciences fields, namely, reviewing standards and practices to assist clients with compliance with governmental laws, regulations and rules pertaining to medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; providing technical regulatory affair consulting services directed to medical, medical technology, biopharmaceutical, and biotechnology companies in order to assure compliance with food and drug administration's laws and regulations; provision of information online pertaining to regulatory compliance in the fields of medical devices, medical technologies, medications, biopharmaceuticals, and biotechnology; and regulatory compliance consulting in the fields of biologics, pharmaceuticals, prescription drugs and medical devices

Consulting services in the fields of biotechnology, pharmaceutical research and development and genetic science; biotechnology research consulting services; pharmaceutical research and product development for use in manufacturing; information technology consultation services; computer aided design services; Consulting services for others in the field of designing pre-clinical and clinical studies and trials for others; product research and development for others in the fields of biologics, pharmaceuticals, prescription drugs and medical devices; quality management services, namely, quality evaluation and analysis, quality assurance and quality control in the field of biologics, pharmaceuticals, prescription drugs and medical devices; scientific consulting and research services relating to the field of pharmaceuticals, medical devices, and life sciences, namely, biology, and medicine; design and development and technical verification consulting services in the fields of biotechnology and pharmaceutical research, and scientific and technological services, namely, scientific research, analysis, testing, and related scientific studies in the field of chemistry and molecular biology, namely, biologics and protein detection, characterization, analysis and testing; Computer consulting services in the field of cloud computing in the field of life science; Technical and scientific research consulting and computer project management for companies in the life sciences fields pertaining to cloud-based data migration; Technical and scientific consulting and management for companies in the life sciences fields pertaining to technical verification and validation laboratory equipment and instrumentation; Technical and scientific consulting and management for companies in the life sciences fields pertaining to digital compression of computer data; Technical and scientific consulting and management for companies in the life sciences fields pertaining to GxP (Good Practice) cloud seeding services; Technical and scientific consulting and management for companies in the life sciences fields for use in the following applications: regulation support; including standard operating procedures, customized compliance training programs, clinical compliance as service (CaaS), medical device cybersecurity, medical device compliance, data integrity, serialization/track and trace, global unique device identification, good clinical practice (GCP) compliance and quality assurance, risk-based monitoring, auditing as a service (AaaS), risk management, remediation planning and execution, emerging companies compliance roadmapping, EU MDR and IVDR compliance, and audits and assessments; Technical and management for companies in the life sciences fields for use in the following applications: supply chain management; including, internet of medical things (IoMT), connected service and quality management, product lifecycle management, product master data management, and enterprise resource planning; Technical and scientific consulting and management for companies in the life sciences fields for use in the following applications: compliance strategy: including laboratory validation, assessments, strategy and remediation planning, performing remediation activities, and providing advisory services to assist GxP labs in meeting commercial and regulatory requirements; Technical and scientific consulting and management for companies in the life sciences fields for use in the following applications: management; including life sciences and program management, GxP cloud services, and organizational change management (OCM)

Filing History

NOTICE OF REGISTRATION CONFIRMATION EMAILED
Jun 28, 2022 NRCC
REGISTERED-PRINCIPAL REGISTER
Jun 28, 2022 R.PR
NOTICE OF ACCEPTANCE OF STATEMENT OF USE E-MAILED
May 27, 2022 SUNA
ALLOWED PRINCIPAL REGISTER - SOU ACCEPTED
May 26, 2022 CNPR
STATEMENT OF USE PROCESSING COMPLETE
Apr 15, 2022 SUPC
CASE ASSIGNED TO INTENT TO USE PARALEGAL
Apr 14, 2022 AITU
USE AMENDMENT FILED
Mar 27, 2022 IUAF
TEAS STATEMENT OF USE RECEIVED
Mar 27, 2022 EISU
NOA E-MAILED - SOU REQUIRED FROM APPLICANT
Sep 28, 2021 NOAM
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
Aug 3, 2021 NPUB
PUBLISHED FOR OPPOSITION
Aug 3, 2021 PUBO
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
Jul 14, 2021 NONP
APPROVED FOR PUB - PRINCIPAL REGISTER
Jun 29, 2021 CNSA
TEAS/EMAIL CORRESPONDENCE ENTERED
Jun 8, 2021 TEME
CORRESPONDENCE RECEIVED IN LAW OFFICE
Jun 7, 2021 CRFA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
Jun 7, 2021 TROA
NOTIFICATION OF NON-FINAL ACTION E-MAILED
Dec 5, 2020 GNRN
NON-FINAL ACTION E-MAILED
Dec 5, 2020 GNRT
NON-FINAL ACTION WRITTEN
Dec 5, 2020 CNRT
TEAS/EMAIL CORRESPONDENCE ENTERED
Oct 28, 2020 TEME
CORRESPONDENCE RECEIVED IN LAW OFFICE
Oct 27, 2020 CRFA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
Oct 27, 2020 TROA
NOTIFICATION OF NON-FINAL ACTION E-MAILED
Oct 15, 2020 GNRN
NON-FINAL ACTION E-MAILED
Oct 15, 2020 GNRT
NON-FINAL ACTION WRITTEN
Oct 15, 2020 CNRT
ASSIGNED TO EXAMINER
Sep 30, 2020 DOCK
NOTICE OF DESIGN SEARCH CODE E-MAILED
Jul 28, 2020 MDSC
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
Jul 27, 2020 NWOS
NEW APPLICATION ENTERED
Jul 2, 2020 NWAP