GLP. The term “GLP” shall mean the then-current good laboratory practice standards promulgated or endorsed by the FDA as defined in 21 C.F.R. Part 58, or the successor thereto, or comparable regulatory standards in jurisdictions outside of the United States as they may be updated from time to time, to the extent such standards are not less stringent than United States standards.
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Sources: Pilot Collaboration and Option Agreement (Synlogic, Inc.)
GLP. The term “"GLP” " shall mean the then-applicable current good laboratory practice standards practices promulgated or endorsed from time to time by the FDA as defined in 21 C.F.R. Part 58accordance with the Act, or the successor thereto, or comparable regulatory standards in jurisdictions outside of the United States as they and which may be updated amended from time to time, to time (or the extent such standards are not less stringent than United States standardsequivalent in any other country).
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