“Good Laboratory Practices” shall mean the current good laboratory practice regulations of the FDA as described in the United States Code of Federal Regulations (“CFR”) or any comparable corresponding foreign regulations or their respective successor regulations.

“Good“Good Laboratory Practices” shall mean the current good laboratory practice regulations of the FDA as described in the United States Code of Federal Regulations (“CFR”) or any comparable corresponding foreign regulations or their respective successor regulations.

“Good Clinical Practices” shall mean the then current good laboratory practice regulations of the FDAGood Clinical Practices as described insuch term is defined from time to time by the United States Code of Federal RegulationsFood and Drug Administration (“CFR”FDA”) or any comparable corresponding foreign regulationsother relevant governmental authority having jurisdiction over the Development, Manufacture or their respective successor regulations.sale of Licensed Product in the Territory pursuant to its regulations, guidelines or otherwise.