Process Over Projects: Rethinking GxP System Validation in an Age of Rapid Change
In today’s rapidly evolving life sciences landscape, treating validation as a series of isolated projects is no longer optimal. In this webinar hosted by Xtalks, our panel of experts discuss the critical importance of treating validation as a core element of an organization’s quality management system (QMS). Integration into the QMS promotes active management of validation activities and deliverables, allowing for the development of metrics for measuring key process indicators (KPI).
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The future of life sciences validation and compliance is not so far away. Already, we are seeing life sciences companies rush to integrate AI where possible, while at the same time striving to manage risk with fewer human and material resources available.
Read the WhitepaperLearn how Nuvolo is leveraging a combination of Sware's Res_Q Platform and expert resources to deliver a fully GxP compliant offering to the life sciences industry, enabling Nuvolo and their customers to meet business goals.
Read the case studyManual computer software validation processes cost life sciences organizations up to 30% in additional project budget. As companies struggle to keep up with a surge of app and software integrations, they incur validation debt: the mounting cost of stretched resources, blanket testing, and missed GxP requirements.
Download the EbookValidation Debt Stops Here
If your organization is ready to embrace the future of life sciences validation, we’re ready to help.