2009-02-262024-05-15https://scholars.lib.ntu.edu.tw/handle/123456789/663415摘要：蒐集、研析與翻譯動物用藥品生體可用率及生體相等性試驗和安定性試驗法規，籌組成立動物用藥品專家委員會，研擬我國動物用藥品生體可用率及生體相等性試驗基準（草案）、以及安定性試驗基準（草案），經委員會討論後，提交共識之草案版本。研析世界各國中草藥檢驗登記和品質基準相關規範，提出我國動物用中草藥管理之建議草案。<br> Abstract: Collect, study and translate regulations for the bioavailability and bioequivalence (BA&BE) study, and stability test for veterinary drugs. Establish an expert committee onveterinary drug regulations for discussing and reviewing the proposed draft guidelines forBA&BE study and stability test. The draft guidelines will be submitted upon conditionthat the committee reaches consensus on the proposed drafts. Study and analyzeregulations for the registration and the quality control specifications for veterinarytranditional and herbal drugs. A draft on the requirement for the registration ofveterinary tranditional and herbal drugs will be proposed.動物用藥品生體可用率及生體相等性安定性試驗動物用中藥veterinary drugbioavailability and bioequivalencestability testveterinary traditional Chinese medicine