AI-Powered Regulatory Compliance

Transform your regulatory compliance with AI-driven insights and automation solutions.

Regulatory Compliance Solutions

Transform your regulatory compliance with AI-powered solutions for GxP, 21 CFR Part 11, and global regulatory requirements. IntuitionLabs helps pharmaceutical companies streamline compliance tracking, automate audit trails, and ensure regulatory adherence across all operations.

Regulatory compliance in pharma

Why Regulatory Compliance Matters in Pharma

The global AI in pharmaceutical market was valued at $1.94 billion in 2025 and is projected to surge to $16.49 billion by 2034, growing at a 27 percent CAGR. IntuitionLabs helps you navigate complex regulatory requirements, automate compliance processes, and maintain audit readiness.

Related topics
GxP Compliance21 CFR Part 11Data PrivacyAudit ManagementDocument Control
  • Ensure compliance with FDA 21 CFR Part 11, HIPAA, and GDPR requirements
  • Automate audit trails and electronic signatures for regulatory documentation
  • Streamline document control and change management processes
  • Maintain data privacy and security across all operations
  • Simplify validation and qualification of computerized systems

Core Capabilities for Regulatory Compliance

GxP Compliance
Comprehensive tools for Good Practice (GxP) compliance, including GMP, GLP, and GCP requirements.
21 CFR Part 11
Automated compliance with FDA electronic records and signatures requirements, including audit trails and system validation.
Data Privacy
Built-in controls for HIPAA, GDPR, and other data privacy regulations, with encryption and access management.
Audit Management
Streamlined audit preparation, execution, and follow-up with automated documentation and tracking.
Document Control
End-to-end document lifecycle management with version control and electronic signatures.
Validation Support
Pre-validated workflows and templates to accelerate system qualification and validation.

Streamline GxP Compliance

Leverage AI to automate compliance tracking, document control, and audit trail management across GxP operations.

GxP compliance streamlining

Simplify 21 CFR Part 11 Compliance

Automate electronic records and signatures management, system validation, and audit trail generation for FDA compliance.

21 CFR Part 11 compliance

Enhance Data Privacy

Implement robust data privacy controls, encryption, and access management to meet HIPAA, GDPR, and other requirements.

Data privacy enhancement

Frequently Asked Questions

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