Lösungen - Produkte

arivis-ClinicalRegulatory

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Clireo eTMF

     Features Overview arivis’ electronic Trial Master File solution - Clireo eTMF - enables companies to easily demonstrate compliance and control over their clinical document... » weiter

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Clireo eDMS

    Features Overview Clireo eDMS is the first document and project management solution designed specifically for the cloud and the needs of life science companies. This revolutionar... » weiter


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Clireo eMPM

       Features Overview Advertising and promoting regulated products requires creative marketing with the additional complexity of requiring compliance with regional and global... » weiter

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Clireo eQMS

       Features Overview Regulated companies must demonstrate that they are in control of their processes and essential documents. arivis Clireo eQMS (electronic Quality Managem... » weiter


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Clireo eCTD

       Features Overview Clireo eCTD provides a validated all-in-one cloud solution for pharmaceutical and biotechnology companies to manage all of their global regulatory activ... » weiter

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Clireo Authoring Templates and Word Toolbar

Features Overview Clireo Authoring Templates and Word Toolbar combine to create a complete authoring framework for the creation of compliant global regulatory submission documents. How it works The... » weiter


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Clireo GxPD - XEVMPD/IDMP

Features Overview Clireo GxPD is a core module based on Microsoft SharePoint. The software suite offers an entire ecosystem for planning, controlling and tracking all notifiable processes in the hi... » weiter

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Clireo GxTRACK (RIMS)

Features Overview In today’s global regulatory environment, Life Sciences companies are challenged with having to manage terabytes of data for products and registrations worldwide as well as ... » weiter