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Secure Science. Protect IP. Govern Health Data.

Discover, classify, and protect sensitive data across R&D, clinical trials, and global operations—while reducing risk, ensuring compliance, and accelerating innovation.

How BigID Helps Pharma & Life Sciences Organizations

  • Scan across clinical, lab, regulatory, and collaboration systems (LIMS, CTMS, Snowflake, SharePoint, AWS)
  • Classify structured + unstructured data: patient data, IP, trial results, contracts, and more
  • Automate compliance with HIPAA, GDPR, GxP, Part 11, and international data regulations
  • Detect overexposed research data and reduce insider and cloud risk
  • Govern AI and analytics with quality, explainable, and compliant data

Why BigID for Pharma & Life Sciences

BigID helps pharma, biotech, medtech, and research institutions discover and protect sensitive data, automate compliance, and manage risk across the full data lifecycle—enabling secure collaboration, faster approvals, and data-driven breakthroughs.

Discover & Classify Clinical, R&D, & Health Data

Automatically find PHI, PII, genomic data, trial records, lab results, and proprietary IP across systems like LIMS, CTMS, file shares, and cloud platforms.

Protect Intellectual Property & Competitive Research

Safeguard patents, formulas, pipeline data, trade secrets, and proprietary documents from leaks, insider threats, and overexposure.

Streamline Compliance (HIPAA, GDPR, GxP, FDA 21 CFR Part 11)

Map and manage data in line with global pharma regulations—automating enforcement and documentation for health data, research, and regulatory submissions.

Govern Clinical Trial Data Across Global Sites

Maintain visibility and control over sensitive trial data shared across CROs, sites, cloud platforms, and external collaborators—ensuring consistency and compliance.

Enable Secure AI, Modeling & Drug Discovery

Ensure training data used in AI models for molecule prediction, trial optimization, or patient stratification is accurate, governed, and free of restricted data.

Automate Data Retention for Regulatory & Research Records

Apply retention and deletion policies to clinical documentation, lab notebooks, and manufacturing records in accordance with GxP and internal standards.

Reduce Legacy Risk Across R&D Systems

Identify ROT, risky data, or outdated records in legacy systems—reducing regulatory risk and simplifying tech consolidation.

Respond Quickly to Audits, FOIA, or Subject Access Requests

Rapidly locate and produce sensitive data for health authorities, regulators, legal holds, or data subject requests—minimizing disruption and ensuring compliance.

Minimize Third-Party Risk in Collaborative Research

Assess how CROs, CDMOs, and research partners access and use your sensitive data—enabling responsible data sharing and stronger data stewardship.

See BigID in Action

Get a personalized demo to see how BigID helps pharma and life sciences leaders protect sensitive data, streamline compliance, and accelerate secure innovation.

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