Securely Streamline Regulatory Communications
ShareVault is the ideal solution for regulatory affairs and regulatory operations professionals needing to share sensitive documents with partners, regulatory advisors, CROs, CMOs and other third parties. Whether you are working to assemble your Electronic Trial Master File (ETMF), or are sharing your Investigational New Drug (IND) application, New Drug Application (NDA), Abbreviated New Drug Application (ANDA), Biologics License Application (BLA), Drug Master File (DMF), Biologics Master File (BMF), Emergency Use Authorization (EUA), any other type of regulatory submission, or confidential documents such as Standard Operating Procedures (SOPs), ShareVault provides an easy-to-use enterprise-grade solution that has not only the best available document control features to keep your information secure, but also includes powerful organizational tools ideally-suited for sharing regulatory submissions and other hierarchical document structures.
We have developed several features specifically for our customers in life sciences. For example, ShareVault preserves the inter-document hyperlinks common in regulatory documents, which is a huge time saver. In addition, ShareVault is the first Virtual Data Room provider to integrate with an eCTD viewer for streamlined viewing of submission documents.
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