Box for life sciences
Innovate faster with seamless collaboration
Powering leading life sciences and biopharma organizations
Now more than ever, we look to life sciences for solutions to improve patient outcomes. But powering innovative molecules and devices across the value chain is difficult with paper-based files, traditional GxP technology, and too many apps. With Box, you speed up R&D workflows, maintain compliance, and reduce your IT footprint — while collaborating on regulated and non-regulated content from a single place.
Speed up CRO exchanges
Collaboration with clinical research organizations (CROs) happens faster on Box, making it easier to work with regulated and non-regulated molecule or device information. Plus, one life sciences cloud gives you more control and coordination with CROs by securely orchestrating content across people outside your organization.
Power secure quality management
Reduce security risks with the regulated content management lifecycle of controlled GxP documents. That includes policies, SOPs, and WIs, all the way from draft to archival. With our modern life sciences cloud stack, you ensure GxP regulated cloud content is always supported.
Keep innovating through M&A
Innovation doesn't have to stop when M&A activities start. Box enables you to accelerate post-merger-integration (PMI) cycle times with faster ingestion of newly acquired regulated and non-regulated R&D information in a secure, GxP environment.
One platform for life sciences
CRO and CMO collaboration
Increase control and coordination with CROs, CMOs, and sponsors. Collaborate on cell data, strategy proposals, and supply chain content with a single source of truth.
M&A post-merger integration
Accelerate M&A and PMI cycle times with faster ingestion of R&D data. Seamlessly transition several terabytes of regulated content.
Commercialization
Accelerate product launches by centralizing digital assets, and collaborate faster on promotional materials across field teams.
Clinical collaboration
Power remote site monitoring and source document verification. Speed up clinical start up by centralizing site feasibility surveys, FDA 1572 forms, and informed consent files.
Quality document management
Manage the lifecycle of a controlled GxP document. Accelerate quality management from draft to disposal on policies, SOPs, and WIs.
Clinical dataset management
Collaborate on SAS datasets across biostatisticians and data management professionals. Securely share regulated datasets between sponsors and CROs.
Simplify content management across your value chain
End-to-end compliance
With Box for life sciences, you accelerate R&D processes with one solution for both regulated and non-regulated life sciences cloud content. And you do it while maintaining 21 CFR Part 11 compliance, along with industry compliance to standards like GxP, HIPAA, GDPR, and DICOM.
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