Adverse Experience Reporting. During the term of the Agreement, each Party shall notify the other immediately of any information (howsoever obtained and from whatever source) concerning any unexpected side effect, injury, toxicity or sensitivity reaction, or any unexpected incidence, and the severity thereof, associated with the clinical uses, studies, investigations, tests and marketing of a PRODUCTS. For purposes of this Section 8.5, "
Appears in 2 contracts
Samples: License Agreement (Drugabuse Sciences Inc), License Agreement (Drugabuse Sciences Inc)
Adverse Experience Reporting. During the term of the Agreement, each Party shall notify the other immediately of any information (howsoever obtained and from whatever source) concerning any unexpected side effect, injury, toxicity or sensitivity reaction, or any unexpected incidence, and the severity thereof, associated with the clinical uses, studies, investigations, tests and marketing of a PRODUCTSProduct or Material. For purposes of this Section 8.5Article 13, "
Appears in 2 contracts
Samples: Option and License Agreement (Corixa Corp), Option and License Agreement (Corixa Corp)
Adverse Experience Reporting. During the term of the Agreement, each Party party shall notify the other immediately of any information (howsoever obtained and from whatever source) concerning any serious or unexpected side effect, injury, toxicity or sensitivity reaction, or any unexpected incidence, and the severity thereof, associated with the clinical uses, studies, investigations, tests and marketing of a PRODUCTSthe Product. For purposes of this Section 8.5Article 13, "
Appears in 2 contracts
Samples: License and Collaboration Agreement (Trinity Medical Group Inc), License and Collaboration Agreement (Trinity Medical Group Inc)
Adverse Experience Reporting. During the term of the Agreement, each Party shall notify the other immediately of any information (howsoever obtained and from whatever source) concerning any unexpected side effect, injury, toxicity or sensitivity reaction, or any unexpected incidence, and the severity thereof, associated with the clinical uses, studies, investigations, tests and marketing of PRODUCTS and, to the extent feasible, any other product containing COMPOUND (hereinafter, a PRODUCTS"PRODUCT"), or COMPOUND. For purposes of this Section 8.5Article 15, "
Appears in 1 contract
Adverse Experience Reporting. During the term of the Agreement, each Party shall notify the other immediately of any information (howsoever obtained and from whatever source) concerning any unexpected side effect, injury, toxicity or sensitivity reaction, or any unexpected incidence, and the severity thereof, associated with the clinical uses, studies, investigations, tests and marketing of PRODUCTS and, to the extent feasible, any other product containing VECTOR (hereinafter, a PRODUCTS"PRODUCT"), or VECTOR. For purposes of this Section 8.5Article 15, "
Appears in 1 contract
