ShareVault’s document security, management and collaboration software enables 100s of our life science customers to protect and manage confidential information in a central repository and eliminates accessing and searching multiple systems within your company to efficiently find, edit, review and share information. ShareVault and its unique life science industry features have been endorsed by the BIO organization and 49 affiliates and used in multiple applications during all growth stages of a life science company as follows:
Secure central repository: mitigate cyber security risks, information leakage, unauthorized access, consolidate information with connectors to BOX, DropBox, SharePoint/Office365, Google Drive and DocuSign.
Business transaction due diligence: M&A, IPO, fund raise, asset sale, technology transfer, licensing
Collaboration & sharing: partnering, vendors, service providers, CROs,CMOs, board members, scientific advisors
Audit and compliance: Unique support for eCTD regulatory submissions and eTMFs, inspection ready, 21CFR11, HIPAA
Med Device regulatory and audit
FDA and regulatory audit and inspection
510(K), PMA document organization, sharing and preparation
Remote clinical trial site monitoring: Reduces trial delays & disruption
New feature: Secure collaborative editing and review workflow option, streamline WORD document updates, reconcile collaborator changes and comments, with detail activity audit trail
Secure central repository: mitigate cyber security risks, information leakage, unauthorized access, consolidate information with connectors to BOX, DropBox, SharePoint/Office365, Google Drive and DocuSign.
Business transaction due diligence: M&A, IPO, fund raise, asset sale, technology transfer, licensing
Collaboration & sharing: partnering, vendors, service providers, CROs,CMOs, board members, scientific advisors
Audit and compliance: Unique support for eCTD regulatory submissions and eTMFs, inspection ready, 21CFR11, HIPAA
Med Device regulatory and audit
FDA and regulatory audit and inspection
510(K), PMA document organization, sharing and preparation
Remote clinical trial site monitoring: Reduces trial delays & disruption
New feature: Secure collaborative editing and review workflow option, streamline WORD document updates, reconcile collaborator changes and comments, with detail activity audit trail
Focus Areas
BIO DOUBLE HELIX SPONSORS
BIO HELIX SPONSORS
