Life Sciences
Your breakthroughs start with
intelligent workflow automation
Securely power life sciences with any AI agent
Life sciences organizations run on research, clinical, commercial, and manufacturing content — but most of its value stays untapped. Box empowers teams to build and govern content-centric processes with any AI agent on a single, GxP-compliant platform. With AI-native automation, 21 CFR Part 11 e-signatures, and large-scale metadata extraction, you can surface insights and automate work across the entire life sciences value chain. See why 2,500+ life sciences customers trust Box.
Collaborate securely,
stay inspection-ready
Your most sensitive content moves between teams, partners, and regulators. Box keeps it controlled with granular permissions, retention policies, and inspection-ready audit trails. Box supports GxP Validation with certified partners to deliver environments that meet FDA, GxP, GDPR, HIPAA, DICOM, and 21 CFR Part 11 requirements.
Turn unstructured
content into insight
90% of enterprise data is unstructured — and in life sciences, most of its value stays untapped. Box AI and Box Extract read across research, clinical, quality, and commercial content to surface insights and turn documents into structured, searchable data. Because Box AI respects your permissions and never trains on your data, every answer is one you can trust.
Fast track workflows
with AI
Put governed content to work. Box automates document routing, reviews, and approvals across research, clinical, manufacturing, and commercial — with 21 CFR Part 11 e-signatures, metadata-driven processing, and secure collaboration built in. Every step stays governed and audit-ready, so teams move faster without adding headcount or risk
Unlimited 21 CFR Part 11 e-signatures
Streamline clinical, R&D, and manufacturing approvals with unlimited, native 21 CFR Part 11 e-signatures—included at no extra cost for GxP customers.
One trusted place for regulated content & AI
Box Hubs turn scattered content into curated knowledge centers for eTMF, study docs, SOPs, and batch records. Query with custom AI agents for instant, permission-aware answers.
Fewer tools. Lower costs. Zero compromise.
Consolidate point solutions with unified, AI-powered storage for regulated and non-regulated content, connected to 1,500+ tools like Salesforce and Microsoft 365.
Protection and govern every file
Govern regulated content with automated retention, legal holds, and defensible disposition. Box Shield adds classification, threat detection, and data-loss prevention, with inspection-ready audit trails for FDA and GxP audits.
Clinical study startup
Automate site feasibility, qualification, and activation with AI-powered routing, e-signatures, and secure external collaboration.
M&A post merger integration
Accelerate M&A and post-merger integration with faster R&D data ingestion and seamless transfer of terabytes of regulated content.
Promotional materials (MLR review)
Accelerate MLR reviews with automated medical, legal, and regulatory routing, real-time tracking, and compliant 2253 filing.
CRO and CDMO collaboration
Collaborate securely with CROs, CDMOs, and sponsors while keeping regulated content controlled, accessible, and governed in one place.
GMP manufacturing & tech transfer
Digitize batch records and streamline tech transfer with governed workflows, 21 CFR Part 11 sign-offs, and full audit traceability.
Electronic Trial Master Files (eTMF)
Centralize and automate eTMF management with structured content, document tracking, secure collaboration, and inspection-ready audit trails.
Secure your most sensitive data
Govern regulated and non-regulated content with retention policies and audit trails, backed by partner-certified validation for GxP, GDPR, HIPAA, DICOM, and 21 CFR Part 11 compliance.