Serial Number
98527726
Owner
XYBION CORPORATIONAttorney
Vanessa A. Ignacio, Esq.Filing Date
Apr 30, 2024
GEMINI LIMS Trademark
Serial Number: 98527726
Trademark Classes
Owner Contact Info
Legal Representation
Correspondence Address
Vanessa A. Ignacio, Esq. Lowenstein Sandler LLP
One Lowenstein Drive
Roseland, NJ 07068
United States
Trademark Details
Filing Date
April 30, 2024
Registration Date
Not Registered
Goods & Services
Downloadable software for laboratory data analysis and management, laboratory sample management, laboratory process and workflow management, laboratory quality assurance management, laboratory instrumentation management, documentation management, invoicing and price quotation management, inventory management, laboratory test management, electronic laboratory notebook management, laboratory execution system management, pharmaceutical product stability studies management, regulatory requirements and best practices management, and creating reports in connection therewith
Software as a service (SAAS) services featuring software for laboratory data analysis and management, laboratory sample management, laboratory process and workflow management, laboratory quality assurance management, laboratory instrumentation management, documentation management, invoicing and price quotation management, inventory management, laboratory test management, electronic laboratory notebook management, laboratory execution system management, pharmaceutical product stability studies management, regulatory requirements and best practices management, and creating reports in connection therewith; Cloud computing featuring software for use in laboratory data analysis and management, laboratory sample management, laboratory process and workflow management, laboratory quality assurance management, laboratory instrumentation management, documentation management, invoicing and price quotation management, inventory management, laboratory test management, electronic laboratory notebook management, laboratory execution system management, pharmaceutical product stability studies management, regulatory requirements and best practices management, and creating reports in connection therewith