GREENLIGHT GURU Trademark
Serial Number: 97711061 • Registration: 7603481
Trademark Classes
Owner Contact Info
Legal Representation
Correspondence Address
Kristin H. Hardy Taft Stettinius & Hollister LLP
115 Madison Street, Suite 700
Dayton, OH 45402
United States
Trademark Details
Filing Date
December 9, 2022
Registration Date
December 17, 2024
Published for Opposition
October 29, 2024
Goods & Services
Business risk management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; business management and consulting services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers for the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing, namely, providing industry expertise and supplier management; records management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers, namely, document indexing for others in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; regulatory information management services for medical device, life science, pharmaceutical, biotech, in vitro diagnostic device, and software as a medical device manufacturers in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing
Consulting services in the field of state and federal regulatory compliance requirements for medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing; Tracking and monitoring regulatory requirements in the fields of medical device manufacturing, life sciences medical device manufacturing, pharmaceutical manufacturing, biotech manufacturing, in vitro diagnostic device manufacturing, and software as a medical device manufacturing for regulatory compliance purposes