Powering leading life sciences and biopharma organizations
Now more than ever, you need to innovate quickly to improve patient outcomes and get new molecules and devices to market faster. Don’t let paper files, legacy GxP technology, and extraneous apps slow you down. With the Content Cloud, you speed up R&D, maintain GxP compliance, and reduce your IT footprint. Plus, collaborate on regulated and non-regulated content from one secure source of truth.
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, 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 one life sciences cloud, 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 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.
Accelerate product launches by centralizing digital assets, and collaborate faster on promotional materials across field teams.
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.