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FDA describes legal limits of drug compounding Agency says few uses allowed for raw active ingredients

机译：FDA描述了药物复合机构的法律限制表示，少量使用原料活性成分

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《Journal of the American Veterinary Medical Association》 |2020年第2期|共3页
作者
Cima Greg;
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正文语种 eng
中图分类动物医学（兽医学）;
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1. FDA describes legal limits of drug compounding Agency says few uses allowed for raw active ingredients [J] . Cima Greg Journal of the American Veterinary Medical Association . 2020,第2期

机译：FDA描述了药物复合机构的法律限制表示，少量使用原料活性成分
2. FDA appeals compounding ruling: Regulatory agency continues to send companies warning letters to stop the compounding of some drugs [J] . DVM Newsmagazine . 2007,第1期

机译：FDA呼吁复利裁决：监管机构继续向公司发送警告信，以停止某些药物的复利
3. Recombinant Drug May Be Rationed; Ranbaxy Still in Trouble with FDA; FDA Joins Nanotechnology Review Body; New HPV Tests Approved; FDA Official Reminds Staff to Protect Information; Anti-IL-6 Drug Linked to Deaths; Genentech Withdraws Raptiva Monoclonal Antibody; FDA Finds Problems with Internet Drug Advertisements [J] . Biotechnology Law Report . 2009,第3期

机译：重组药物可按比例分配； Ranbaxy仍在与FDA纠缠； FDA加入纳米技术审查机构；批准了新的HPV测试； FDA官员提醒员工保护信息；抗IL-6药物与死亡有关； Genentech撤回Raptiva单克隆抗体； FDA发现互联网药品广告存在问题
4. Impact of the Detection and Quantitation Limits on the Analytical Feasibility of Measuring the European Chemicals Agency Risk Assessment Committee's Recommendations for Occupational Exposure Limit Values for Nickel and Its Compounds in the Workplace [C] . Steven Verpaele Symposium on detection limits in air quality and environmental measurements . 2019

机译：检测和定量限制对测量欧洲化学物质机构风险评估委员会的分析可行性的分析可行性，为镍及其化合物在工作场所的职业暴露限制值
5. Identification of the most aroma-active compounds in strawberries: Variety differences and the effects of heating on strawberry puree. [D] . Schulbach, Kurt Frederick. 2002

机译：鉴定草莓中最具香气活性的化合物：品种差异和加热对草莓泥的影响。
6. The Stereoselective Nitro-Mannich Reaction in the Synthesis of Active Pharmaceutical Ingredients and Other Biologically Active Compounds [O] . Ana Maria Faisca Phillips, M. Fátima C. Guedes da Silva, Armando J. L. Pombeiro 2020

机译：活性药物成分和其他生物活性化合物的合成中的立体选择性硝基曼尼希反应
7. PHP22 Evaluating Criticism Of The Fda Accelerated Approval Pathway - Ema Evaluation Of Drugs That Have Been Withdrawn Following Accelerated Approval By The Fda [O] . Macaulay R. 2014

机译：PHP22评估对Fda加速批准途径的批评-Ema评估Fda加速批准后撤回的药物

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