Box for life sciences

Innovate faster with seamless collaboration

Life Sciences

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.

 

Med-el
AstraZeneca
IQVIA
Medtronic
Amgen
ICON logo

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 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

collaboration
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.

integration
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.

teams
Commercialization

Accelerate product launches by centralizing digital assets, and collaborate faster on promotional materials across field teams.

documents
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.

GxP document
Quality document management

Manage the lifecycle of a controlled GxP document. Accelerate quality management from draft to disposal on policies, SOPs, and WIs.

dataset
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

clinical
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.

Protect clinical content
quality
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

Read ebook
pills
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.

See how AstraZeneca powers innovation

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

innovate for life sciences
Eliminate silos across all workflows, from R&D to commercialization

Learn how Box accelerates the way you innovate for life sciences content management.

Read ebook
gxp
The Content Cloud for GxP Compliance

Get your therapies to market faster, simplify workflows, and stay compliant.

Read datasheet

Ready to get started?