STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior to the First Commercial Sale, the Licensee agrees to provide the IC with reasonable quantities of Licensed Products or materials made through the Licensed Processes for the IC’s research use.
Appears in 8 contracts
Samples: Patent License Agreement (PDS Biotechnology Corp), Patent License Agreement, Patent License Agreement (GeoVax Labs, Inc.)
STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior Upon request and prior to the First Commercial Sale, the Licensee agrees to require the Sublicensee to provide the IC with reasonable quantities of Licensed Products or materials made through the Licensed Processes for the IC’s IC research use.
Appears in 3 contracts
Samples: Public Health Service, Public Health Service, Public Health Service
STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior to the First Commercial Sale, the Licensee agrees to provide the IC with reasonable quantities of Licensed Products or materials made through the Licensed Processes for the IC’s research use. The Licensee agrees that products used or sold in the United States embodying Licensed Products or produced through use of Licensed Processes shall be manufactured substantially in the United States, unless a written waiver is obtained in advance from the IC.
Appears in 3 contracts
Samples: Public Health Service, Public Health Service, Public Health Service
STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior to the First Commercial Sale, the Licensee agrees to provide the IC with reasonable quantities of Licensed Products or materials made through the Licensed Processes for the IC’s IC research use.
Appears in 2 contracts
Samples: Public Health Service, Public Health Service
STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior to the First Commercial Sale, and unless prohibited by law, upon specific written request by the IC, the Licensee agrees to provide the IC with commercially reasonable quantities of Licensed Products or materials made through the Licensed Processes and in Licensee's possession for IC in vitro research use provided that the IC’s research use.:
Appears in 1 contract
STATUTORY AND NIH REQUIREMENTS AND RESERVED GOVERNMENT RIGHTS. 5.1 Prior to the First Commercial Sale, the Licensee agrees to provide the IC with reasonable quantities of Licensed Products or materials made through the Licensed Processes for the IC’s non-clinical research use.
Appears in 1 contract
Samples: Patent License Agreement Nonexclusive Sublicensable (Generation Bio Co.)
