Sisthema - Società di servizi per il mondo Life Science - Sisthema srl - Audit, Taratura e Convalida, Consulenza e Formazione

Il nuovo EU GMP Annex 1: le principali novità sui requisiti per la produzione di medicinali sterili

11/25/2020

https://www.sisthema.biz/wp-content/uploads/2020/11/20201125-sisthema-newsletter-vert.jpg 760 524 adm-sisthema https://www.sisthema.biz/wp-content/uploads/2022/01/eurofins-sisthema-300x59.png 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

Gli Indicatori di Qualità come Strumento di Controllo

09/28/2020

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Commissioning & Qualification: Il ruolo del Validation Engineer tra regole e creatività

07/15/2020

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Estate: logistica del farmaco e mappatura della temperatura

06/26/2020

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Remote Audit

05/12/2020

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ICH vs APS Stability Traditional Approach vs Accelerated Predictive Stability

04/29/2020

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TRAINING: we have improved new Training methods

04/23/2020

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AUDIT: we have increased our Auditors' network

04/23/2020

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