{"id":18098,"date":"2015-05-14T17:14:54","date_gmt":"2015-05-14T21:14:54","guid":{"rendered":"http:\/\/wwwdev.veeva.com\/?post_type=products&p=18098"},"modified":"2015-08-27T12:33:38","modified_gmt":"2015-08-27T16:33:38","slug":"vault-rim","status":"publish","type":"products","link":"https:\/\/www.veeva.com\/cn\/product\/vault-rim\/","title":{"rendered":"Vault RIM"},"content":{"rendered":"
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\nHome<\/a> · R&D Solutions<\/a><\/span> · Vault RIM<\/span>\n<\/div>\n

Next Generation RIM<\/h2>\n

Get the latest industry report on the current state of RIM, trends, and projected changes for the RIM landscape.\n<\/p>\nDownload Report<\/span><\/a>\n

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R&D Cloud<\/div>\n

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Vault ETMF<\/div>\n

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Vault QualityDocs<\/div>\n

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Vault Submissions<\/div>\n

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Vault RIM<\/div>\n

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Vault Platform<\/div>\n

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Veeva Vault RIM \u2013 Planned for Availability Q1 2016<\/h1>\n

A global authoritative source for all regulatory content and product registration data.<\/p>\n

Veeva Vault RIM is a suite of applications providing fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission document management, submission archiving, health authority correspondence and commitments, and product registration management.<\/p>\n

The visibility that results from a unified solution will streamline global processes, helping life sciences companies respond faster to business changes, compliance concerns, and health authority requests.<\/p>\n

BENEFITS<\/h5>\n