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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As the life sciences landscape rapidly evolves, technology adoption demands agile validation methods to maintain GxP compliance. Learn how organizations can shift from project-based validation to a process-driven approach, integrating validation into their Quality Management System.
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.