對生物樣品中的外源生物和生物制劑進行選擇性、敏感性和可重復(fù)性分析，從而獲得可靠的數(shù)據(jù)，這是每一個成功的藥物開發(fā)項目的基礎(chǔ)和關(guān)鍵部分。同樣的原則也可以應(yīng)用于許多其他領(lǐng)域的研究，如法醫(yī)學、毒理學和體育興奮劑檢測?！渡锓治觥奉I(lǐng)域結(jié)合了復(fù)雜的技術(shù)，將樣品制備和先進的分離技術(shù)與MS和NMR檢測系統(tǒng)、自動化和機器人技術(shù)相結(jié)合。監(jiān)管機構(gòu)制定的有關(guān)方法開發(fā)和驗證的標準越來越多地界定了速度和質(zhì)量之間的界限?！渡锓治觥肥且婚T進步的學科，未來將有許多令人興奮的機會進一步減少樣本量、分析成本和環(huán)境影響，以及提高靈敏度、特異性、準確性、效率、分析吞吐量、數(shù)據(jù)質(zhì)量、數(shù)據(jù)處理和處理?！渡锓治觥冯s志側(cè)重于檢測或定量研究人類或動物生物樣品中分析物的技術(shù)和方法。生物分析鼓勵提交描述前瞻性應(yīng)用的文章，包括生物傳感器、微流體、微型化分析設(shè)備和新的連字符和多維技術(shù)。生物分析以簡潔、一目了然的文章格式提供基本信息。該領(lǐng)域的關(guān)鍵進展由國際專家進行報告和分析，為現(xiàn)代生物分析學家提供了一個權(quán)威而又容易接近的論壇。主要的主題包括：分析物提取和樣品制備，包括微取樣色譜與分離科學MS、NMR等關(guān)鍵檢測方法，包括配體結(jié)合檢測藥物和代謝物分析生物標志物檢測、診斷檢測和檢測試劑盒方法開發(fā)和驗證方法創(chuàng)新的生物分析方法和新的儀器設(shè)備實驗室自動化及效率規(guī)管及遵從問題數(shù)據(jù)處理及管理

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