Box for life sciences
Innovate faster with seamless collaboration
Unlock the value of life sciences and biopharma content
Fragmented systems create bottlenecks in hiring, onboarding, clinical trials, and regulatory submissions. With Intelligent Content Management from Box, workflows are simplified and streamlined by providing a secure, unified source of truth for both regulated and non-regulated content. Bring therapies to market faster by accelerating R&D while maintaining GxP compliance and reducing your IT footprint. With built-in AI, gain actionable insights and mitigate risks, while fostering smarter collaboration. See why 2,200+ life sciences customers trust Box.
Comply with critical regulations
With Box for life sciences, you accelerate R&D with one solution for both regulated and non-regulated life sciences cloud content. Maintain 21 CFR Part 11 compliance for electronic records and e-signatures, along with industry compliance across standards like GxP, HIPAA, GDPR, and DICOM.
Speed up CRO exchanges
Share regulated and non-regulated molecule and device information faster with clinical research organizations (CROs). With an Intelligent Content Management platform, you enhance content collaboration and control — and share it securely with external teams.
Enhance quality management
Reduce security risks with regulated content management for the entire data lifecycle (from drafts to archiving) for controlled GxP documents. With a modern life sciences cloud stack, you get the support you need for GxP-regulated cloud content such as policies, SOPs, and WIs.
Maintain your momentum
Innovation doesn't have to stop when M&A activities start. 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 Intelligent Content Management 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.
Intelligent Content Management across your value chain
Clinical
Speed up R&D processes across life sciences organizations by streamlining collaboration and the exchange of regulated and non-regulated molecule and device information throughout clinical operations.
Quality
Reduce risk by managing quality documents, from procedures to educational material across quality and regulatory teams. Plus, Box partners create a cohesive document management quality solution.
Commercial
Get to market faster by collaborating in real time on FDA-approved collateral across marketing and field sales teams. Box streamlines life sciences content management as content flows inside and outside your organization.
Enable FDA-compliant e-signatures
Transform and automate your signature and approval workflows across the organization - from clinical trial enrollment and new drug applications to R&D documentation and manufacturing.
Box supports 21 CFR Part 11 compliance for both electronic records and unlimited e-signatures, providing the most comprehensive solution to boost efficiency, drive productivity, and digitally transform your life sciences workflows. GxP Validation customers can leverage unlimited, native e-signatures for 21 CFR Part 11 compliance at no additional cost — avoiding the high costs associated with standalone e-signature providers.
Resources
Eliminate silos across all workflows, from R&D to commercialization
Learn how Box accelerates the way you innovate for life sciences content management.
Intelligent Content Management for GxP Compliance
Get your therapies to market faster, simplify workflows, and stay compliant.