We have independent QA & QC dept., responsible for quality assurance and quality control.
There are11persons in QA and 38persons in QC.
設(shè)有獨(dú)立的QA和QC部門,履行質(zhì)量保證和質(zhì)量控制職責(zé)。現(xiàn)有人員QA11人, QC 38人。
Our company devotes to improving pharmaceutical quality management system continuously, focus on total quality management and quality risk management. Procedures were established, such as supplier audit, material & product release, stability test, market service, change control, deviation investigation, CAPA, quality review etc. Risk evaluation and control take place at each step to prevent quality accidents actively.
致力于不斷完善藥品質(zhì)量管理體系,注重生產(chǎn)全過程質(zhì)量管理和藥品質(zhì)量風(fēng)險(xiǎn)管理。建立了供應(yīng)商審計(jì)、
物料和產(chǎn)品放行、穩(wěn)定性考察、市場(chǎng)服務(wù)、變更控制、偏差調(diào)查、糾正預(yù)防措施和年度質(zhì)量回顧等制度,
對(duì)各環(huán)節(jié)可能出現(xiàn)的風(fēng)險(xiǎn)進(jìn)行評(píng)估和控制,主動(dòng)防范質(zhì)量事故的發(fā)生。
公司質(zhì)量控制部配備有豐富GMP和檢驗(yàn)技術(shù)經(jīng)驗(yàn)的技術(shù)人員以及先進(jìn)的檢驗(yàn)儀器,能夠很好地完成國內(nèi)外對(duì)產(chǎn)品質(zhì)量要求的檢驗(yàn)工作。
浙江耐司康藥業(yè)有限公司 版權(quán)所有(C)2019 網(wǎng)絡(luò)支持
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