VEEVA (Class 99)

The trademark application number 8108019 is currently marked as "New Application" in the official trademark registry.

The trademark application number 8108019 is owned by Veeva Systems Inc..

Trademark application number 8108019 is filed under Class 99, which relates to the specified goods and services.

Trademark application number 8108019 relates to "[CLASS : 41] Education and training services, namely, arranging and conducting in-person and online classes, workshops, training sessions, seminars, conferences, webinars, and symposiums in the fields of life sciences, pharmaceuticals, biotechnology, medical devices, clinical operations, clinical data management, regulatory affairs, quality management, pharmacovigilance, medical affairs, commercial operations, and regulatory compliance; providing training for certification in the fields of life sciences, pharmaceuticals, biotechnology, medical devices, clinical operations, clinical data management, regulatory affairs, quality management, pharmacovigilance, medical affairs, commercial operations, and regulatory compliance; providing educational examination for certification in the of life sciences, pharmaceuticals, biotechnology, medical devices, clinical operations, clinical data management, regulatory affairs, quality management, pharmacovigilance, medical affairs, commercial operations, and regulatory compliance; providing a learning management system (LMS) to ensure and assess training compliance, qualification, and job readiness in the life sciences industry (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); providing online, non-downloadable electronic publications in the nature of blogs, articles, white papers, and reports in the field of life sciences, pharmaceuticals, biotechnology, medical devices, and consumer products; educational services, namely providing training of teachers, instructors, and educators, in fields of life sciences, pharmaceuticals, biotechnology, medical devices, clinical operations, clinical data management, regulatory affairs, quality management, pharmacovigilance, medical affairs, commercial operations, and regulatory compliance; providing training in the field of determining compliance with certification standards of others; education services, namely, training educators in the fields of determining compliance with certification standards; testing, analysis, and evaluation of the knowledge, skills and abilities of others in the field of teaching others; providing authorized training partner programs to establish a measure of quality and continued governance of others to teach education courses. [CLASS : 42] Software as a service (SaaS), data as a service (DaaS), and platform as a service (PaaS) services featuring non-downloadable computer software, including non-downloadable mobile applications, for use by the life sciences, pharmaceutical, biotechnology, medical device, and consumer products industries; software as a service (SaaS), data as a service (DaaS) and platform as a service (PaaS) services featuring non-downloadable software using artificial intelligence (AI), generative artificial intelligence, large language models (LLMs), machine learning (ML), predictive analytics, data analytics, and intelligent software agents (bots) for use in customer relationship management (CRM), patient relationship management, sales force automation and effectiveness, marketing automation, managing, planning, and executing customer interactions, omnichannel communications, live events, virtual events, and hybrid events, clinical operations and clinical trial management, namely, managing, tracking, and organizing clinical trials, study startup, electronic trial master files (eTMF), site activation, randomization and trial supply management (RTSM), clinical trial disclosures, and clinical trial payments, clinical data management, namely, electronic data capture (EDC), building and managing clinical studies, aggregating, cleaning, and transforming clinical data from multiple sources, and capturing patient data, electronic clinical outcome assessments (eCOA), and patient-reported outcomes, regulatory affairs and regulatory information management (RIM), namely, managing, planning, tracking, and reporting on product registrations, submissions, health authority interactions, regulatory content, and submissions archives, quality management (QMS), namely, managing quality processes, GxP documents, compliant content, validation, validation management, and compliance training, laboratory information management (LIMS), namely, managing and optimizing quality control (QC) laboratory operations, batch release management, namely, the aggregation, review, and traceability of batch-related data and content, pharmacovigilance and drug safety, namely, adverse event management, managing safety content, safety signal detection and management, and advanced reporting and analysis, management of commercial, medical, and promotional content, including creation, review, approval, distribution, and digital asset management (DAM) of compliant promotional and medical materials, generating, managing, and providing privacy-safe analytics, namely, data analytics that connect advertising campaigns to business outcomes using health data in a privacy-safe way, and segmented analytics which connect healthcare marketers to their target audiences through advertising in a privacy-safe way, master data management (MDM) of customer, product, and reference data, territory and sales roster planning and alignment; providing an online, non-downloadable, searchable database featuring projected data and anonymous patient longitudinal data (APLD), including dispensed prescription claims, medical claims, and retail and non-retail medical products (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); providing an online, non-downloadable, searchable database featuring projected prescription claims and medical claims at the health care provider (HCP), health care organization (HCO), ZIP, state, and national level for retail and non-retail medical products (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); providing a low-code development platform and software development tools for building, customizing, extending, and integrating software applications; providing an online, non-downloadable, searchable database featuring medical, scientific, and commercial data for scientific and medical research purposes, namely, data regarding clinical trials, medical research, healthcare providers (HCPs), healthcare organizations (HCOs), key opinion leaders (KOLs), and anonymized longitudinal patient data (APLD); computer services, namely, integration of computer software and data; IT consulting services; design and development of computer hardware and software; technical support services, namely, troubleshooting of computer software problems; providing software as a service (SaaS), namely, featuring software for the access, management, organization, collaboration, and sharing of content, communications, electronic data, and information in the fields of customer relationship management (CRM), content management, and life sciences clinical trial document collection, management, and analysis; providing software as a service (SaaS) featuring software for document management; software as a service (SAAS) services featuring software for the collection, editing, managing, organizing, modifying, bookmarking, transmission storage and sharing of data and information; software as a service (SAAS) services featuring software for providing users the ability to create, modify, edit, share, manage, store, and view electronic media or information over the Internet or other communications network; software as a service (SAAS) for use in customer relationship management (CRM); software as a service (SAAS) for maintaining document control; software as a service (SAAS) services for document management and content management; software as a service (SAAS) featuring quality management software; providing temporary use of non-downloadable software used to perform quality control management of business operations; computer services, namely, providing temporary use of non-downloadable software for users to create, edit, manage, store, retrieve, access, track, profile, categorize, search, publish, archive, deliver, administer, modify and control files, text, images, electronic content, and data; platform as a service (PAAS) featuring computer software platforms for data management; computer services, namely, online portal services, namely, providing temporary use of on-line non-downloadable software development tools; platform as a service (PAAS) services featuring computer software platforms for use in the creation, development, operation and testing of software applications; all of the foregoing for the purposes of providing solutions for the management of clinical trial documents, regulatory documents and filings and submissions, quality management documentation and claims management documentation, and for the purposes of providing solutions for customer relationship management (CRM). [CLASS : 9] Downloadable computer software and downloadable mobile applications for use by the life sciences, pharmaceutical, biotechnology, medical device, and consumer products industries; downloadable computer software and downloadable mobile applications featuring artificial intelligence (AI), generative artificial intelligence, machine learning, predictive analytics, data analytics, and intelligent software agents (bots) for use in customer relationship management (CRM), patient relationship management, sales force automation and effectiveness, marketing automation, managing, planning, and executing customer engagement, omnichannel communications, and live, virtual, and hybrid events, clinical operations and clinical trial management, namely, managing, tracking, and organizing clinical trials, study startup, electronic trial master files (eTMF), site activation, randomization and trial supply management, clinical trial disclosures, and clinical trial payments, clinical data management, namely, electronic data capture (EDC), building and managing clinical studies, aggregating, cleaning, and transforming clinical data from multiple sources, and capturing patient data, electronic clinical outcome assessments (eCOA), and patient-reported outcomes, regulatory affairs and regulatory information management (RIM), namely, managing, planning, tracking, and reporting on product registrations, submissions, health authority interactions, regulatory content, and submissions archives, quality management (QMS), namely, managing quality processes, GxP documents, compliant content, validation, validation management, and compliance training, logging, creating, viewing, searching, and submitting quality events, non-conformance reports (NCRs), and incidents, and capturing and adding photographic and visual evidence to quality records, pharmacovigilance and drug safety, namely, adverse event management, managing safety content, safety signal detection and management, and advanced reporting and analysis, management of commercial, medical, and promotional content, including creation, review, approval, distribution, and digital asset management (DAM) of compliant promotional and medical materials, master data management (MDM) of customer, product, and reference data, territory and sales roster planning and alignment, digital engagement and omnichannel communications between life sciences company representatives and healthcare professionals, scheduling and conducting remote meetings and video calls, secure and compliant chat and messaging, sharing, viewing, and receiving approved promotional and medical content and patient resources, and for requesting samples and capturing electronic signatures remotely, performing internal and external audits, namely, for downloading, accessing, completing, and submitting audit checklists authored in a central database, capturing and recording audit findings, observations, and comments, and for attaching supporting evidence, including photos, videos, and files, to audit records; downloadable software development tools; downloadable searchable electronic files and databases for use with computer software, featuring medical, scientific, and commercial data for scientific and medical research purposes, namely, data regarding clinical trials, medical research, healthcare providers (HCPs), healthcare organizations (HCOs), key opinion leaders (KOLs), and anonymized longitudinal patient data (APLD); computer software and mobile application software for the access, management, organization, collaboration, and sharing of content, communications, electronic data, and information in the fields of customer relationship management (CRM), content management, and life sciences clinical trial document collection, management, and analysis; computer software and mobile application software for document management; computer software and mobile application software for the collection, editing, managing, organizing, modifying, bookmarking, transmission storage and sharing of data and information; computer software and mobile application software for the collection, editing, managing, organizing, modifying, bookmarking, transmission storage and sharing of clinical data and information; computer software and mobile application software for providing users the ability to create, modify, edit, share, manage, store, and view electronic media or information over the Internet or other communications network; computer software and mobile application software for use in customer relationship management (CRM); computer software and mobile application software for maintaining document control; computer software and mobile application software for document management and content management; computer software and mobile application quality management software; computer software and mobile application software for performing quality control management of business operations; computer services, namely, computer software and mobile application software for users to create, edit, manage, store, retrieve, access, track, profile, categorize, search, publish, archive, deliver, administer, modify and control files, text, images, electronic content, data, and clinical data; computer software and mobile application software for data management; computer software and mobile application software for clinical data management; software development kits (SDK); computer software and mobile application software for use in the creation, development, operation and testing of software applications; all of the foregoing for the purposes of providing solutions for the management of clinical trial documents, regulatory documents and filings and submissions, quality management documentation and claims management documentation, and for the purposes of providing solutions for customer relationship management ("CRM"). [CLASS : 35] Business management consulting; business strategic advisory services; business consulting, management, and planning services in the field life sciences, pharmaceutical, biotechnology, and medical device industries; advertising, marketing, and promotional services; advertising and marketing analytics services, namely, measuring, analyzing, and optimizing the effectiveness of direct-to-consumer and healthcare professional (hcp) digital, television, and print advertising campaigns for others; providing business insights by connecting advertising campaign exposures to health data and business outcomes; market research and business research services for the life sciences, pharmaceutical, biotechnology, and medical device industries, namely, providing business data, business intelligence, and business data analytics; business services, namely, compilation, systematization, and management of data and information into computer databases for business and commercial purposes; providing business data, namely, providing online searchable databases featuring commercial and business data, including profiles of healthcare professionals (HCPs) and healthcare organizations (HCOs), key opinion leaders (KOLs), HCP engagement and access metrics, anonymized longitudinal patient data (APLD), and projected patient and prescriber data for use in business and market research, commercial targeting, and sales and marketing segmentation (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); providing a website featuring business and commercial information in the field of life sciences (term considered too vague by the International Bureau pursuant to Rule 13 (2) (b) of the Regulations); compilation of statistics for business purposes.".