Good Laboratory Practice or GLP

Example Definitions of "Good Laboratory Practice or GLP"
Good Laboratory Practice or GLP. The term "Good Laboratory Practice" or "GLP" means the then-current Good Laboratory Practice Standards promulgated or endorsed by the U.S. Food and Drug Administration or in the case of any other country in the Territory, comparable regulatory standards promulgated or endorsed by that country, including those procedures expressed in or contemplated by any Regulatory Filings.
Found in Enumeral Biomedical Holdings, Inc. contract
Good Laboratory Practice or GLP. The term "Good Laboratory Practice" or "GLP" means the then-current Good Laboratory Practice Standards promulgated or endorsed by the U.S. Food and Drug Administration FDA or in the case of any other country in the Territory, comparable regulatory standards promulgated or endorsed by that country, including those procedures expressed in or contemplated by any Regulatory Filings. regulatory filings.
Found in PIERIS PHARMACEUTICALS, INC. contract
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Good Laboratory Practice or GLP. Means the then-current standards for laboratory activities for pharmaceuticals, as set forth in the FD&C Act and such standards of good laboratory practice as are required by the European Union and other organizations and governmental agencies in countries in which the Product is intended to be sold, to the extent such standards are not in contravention with United States GLP.
Found in Synovics Pharmaceuticals contract
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