Serial Number
77364597
Owner
Allphase Clinical Research Services Inc.Attorney
Mary Margaret L. O'DonnellFirst Use Date
Feb 28, 2007
Filing Date
Jan 4, 2008
EXCEEDING YOUR EXPECTATIONS Trademark
Serial Number: 77364597 • Registration: 3702365
Trademark Classes
Class 39 - Transportation & Storage
Transport; packaging and storage of goods; travel arrangement
Class 41 - Education & Entertainment
Education; providing of training; entertainment; sporting and cultural activities
Class 42 - Computer & Scientific
Scientific and technological services; industrial analysis and research services
Class 45 - Legal & Security Services
Legal services; security services for the protection of property and individuals
Class 35 - Advertising & Business
Advertising; business management; business administration; office functions
Owner Contact Info
Legal Representation
Trademark Details
Filing Date
January 4, 2008
Registration Date
October 27, 2009
First Use Anywhere
February 28, 2007
First Use in Commerce
February 28, 2007
Published for Opposition
November 25, 2008
Goods & Services
Providing training in the field of clinical trials and clinical trial management for the pharmaceutical and biotechnological industries
Clinical supply storage in the field of clinical and medical supplies
Pre-clinical to phase four clinical trial management services, namely, pre-study document collection and review, site selection, visits and audits, site compliance, project tracking and monitoring reports, negotiation and administration of investigator grants, labeling, packaging, distribution, coordination and tracking of clinical trial products and materials, regulatory document processing, central laboratory selection and coordination; pre-clinical to phase four clinical trial management services, namely, managing site and study-specific subject recruitment strategies and programs in the nature of contingency strategies and solutions to address specific project challenges; pre-clinical to phase four clinical trial management services, namely, managing the development of all study related documents and materials in the nature of study protocols, amendments, paper and electronic case report forms, informed consent forms, diary cards, safety narratives, presentation posters, technical briefs and training manuals; pre-clinical to phase four clinical trial management services, namely, managing all aspects of study, drug reconciliation, and inventory and distribution reports, managing all aspects of clinical trials, namely, managing investigators, technicians, and participants, ethical reviews, investigator meetings, databases, statistical analyses and reporting, randomization logistics, medical writing services, recruitment of investigators, technicians and participants; providing data management services in the medical, pharmaceutical and biotechnological field
Regulatory affairs, namely, reviewing standards and practices to assure compliance with clinical trial laws and regulations
Medical and scientific research consulting regarding pre-clinical to phase four clinical trials; providing quality assurance services in the pharmaceutical and biotechnological industries
