{"id":20551,"date":"2023-10-27T11:28:53","date_gmt":"2023-10-27T11:28:53","guid":{"rendered":"https:\/\/clinlabint.com\/?p=20551"},"modified":"2023-10-27T11:56:37","modified_gmt":"2023-10-27T11:56:37","slug":"kivo-unveils-kivo-go-document-management-solution-for-smaller-teams","status":"publish","type":"post","link":"https:\/\/clinlabint.com\/kivo-unveils-kivo-go-document-management-solution-for-smaller-teams\/","title":{"rendered":"Kivo unveils Kivo GO Document Management Solution for smaller teams"},"content":{"rendered":"
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Kivo unveils Kivo GO Document Management Solution for smaller teams<\/h1>\/ in Product News<\/a> <\/span><\/span><\/header>\n<\/div><\/section>
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Kivo, the intuitive Document Management Solution for life sciences, has introduced Kivo GO, a unified platform for emerging life sciences teams who need to work together efficiently across all functions while maintaining compliance and security.<\/strong><\/p>\n

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The majority of new drugs and devices in development are being managed by emerging companies working carefully \u2013 and in compliance with regulatory authorities \u2013 through trials and approvals. This requires close collaboration between their Regulatory, Clinical, and Quality teams \u2013 and valuable time is often lost due to patchwork systems, manual processes and avoidable delays. A recent McKinsey study estimates the value of each day of delay at $1 million in lost revenue potential.<\/p>\n<\/div><\/section>
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\u201cWhen it comes to advancing a new treatment, time to market is critical, both for the patients who need it and the company sponsoring it,” said Toban Zolman, Kivo\u2019s CEO. \u201cHowever, these smaller Regulatory, Clinical and Quality teams often don\u2019t have the budget or admin resources for an \u2018enterprise\u2019 solution \u2013 so they lose a shocking amount of time trying to manage documents and processes in a compliant way.\u201d<\/p>\n

Kivo offers these teams a fit-for-purpose solution to accelerate their timelines with the launch of Kivo GO \u2013 a compliant collaboration solution with built-in modules for every function including RIM, eTMF, and QMS. Key benefits of the Kivo solution include:<\/p>\n

\u2022 Fast, simple, intuitive:<\/strong> Kivo GO allows Regulatory, Clinical, and Quality teams to work together easily \u2013 including with their partners and vendors \u2013 all in the same secure workspace. Functional modules such as eTMF, RIM, QMS, an eCTD viewer, and more are all part of the same platform \u2013 no integrations required.<\/p>\n

\u2022 Designed (and priced) for smaller teams:<\/strong> Scaling teams no longer need to choose between patchwork systems or a big-budget solution. With Kivo, everything is included for one affordable price \u2013 fast setup, lifetime updates, real-time support \u2013 and everyone on the team can access the same workspace and functional modules.<\/p>\n

\u2022 Best-in-class security & compliance:<\/strong> Kivo GO is Part 11 Compliant and Validated \u2013 with no local installation required and built-in support for Single Sign-On. Kivo is a fit-for-purpose, cloud-based system with automatic guardrails and audit trails to safeguard data and keep everyone in compliance.<\/p>\n

\u2022 New quality management (QMS) features:<\/strong> The launch includes the expansion of Kivo\u2019s QMS capabilities, with new modules for SOPs and Controlled Documents, Training, CAPAs, Vendor Management, Audits, and more. These all leverage the templates, workflows, reporting & project management built into the Kivo GO platform. The Kivo GO platform also extends to vendors and partners, such as CROs and regulatory consultants. By leveraging Kivo across their sponsor projects, these services providers can standardize their process and project management \u2013 working more efficiently and consistently with their sponsor teams.<\/p>\n

For more information, visit: https:\/\/kivo.io<\/a><\/strong><\/p>\n

Digital issue: Please click here<\/a> for more information<\/p>\n<\/div><\/section>
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