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adm-sisthema2020-11-25 14:35:042020-11-25 15:06:55Il nuovo EU GMP Annex 1: le principali novità sui requisiti per la produzione di medicinali sterili
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adm-sisthema2020-11-25 14:35:042020-11-25 15:06:55Il nuovo EU GMP Annex 1: le principali novità sui requisiti per la produzione di medicinali sterili
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adm-sisthema2020-09-28 10:49:372020-09-29 11:41:17Gli Indicatori di Qualità come Strumento di Controllo
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adm-sisthema2020-07-15 17:09:522020-07-21 10:24:18Commissioning & Qualification: Il ruolo del Validation Engineer tra regole e creatività
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adm-sisthema2020-06-26 10:17:522020-07-15 17:10:44Estate: logistica del farmaco e mappatura della temperatura
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adm-sisthema2020-05-12 09:08:212020-05-12 10:42:09Remote Audit
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adm-sisthema2020-04-29 08:51:232020-04-29 18:36:32ICH vs APS Stability Traditional Approach vs Accelerated Predictive Stability
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adm-sisthema2020-04-23 08:22:202020-04-23 09:48:00TRAINING: we have improved new Training methods
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adm-sisthema2020-04-23 08:12:012020-04-30 15:30:06AUDIT: we have increased our Auditors' network
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adm-sisthema2019-11-04 09:03:132020-03-13 13:47:34Sisthema e Chiman valutazione e dosaggio di impurezze genotossiche
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adm-sisthema2019-05-03 09:04:532020-03-13 13:50:43Sisthema partecipa al 59° simposio AFI
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adm-sisthema2019-02-15 09:09:012020-03-13 13:59:36Sisthema partecipa a CLEAN ROOM 2019Corporate brochure
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