Managing Compliance Risk in Life Sciences: How Can IT & Quality Teams Root It Out
Making the jump from CSV to CSA will require close collaboration between IT and Quality teams – and a solid understanding of the role future technologies will play. Join our expert panel for an engaging webinar, hosted by Xtalks, to learn more about the key role collaboration, technology, and market forces will play in tomorrow's compliance landscape.
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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.