Resources

Compliance Knowledge & Tools

Access whitepapers, case studies, webinars, API documentation, and our comprehensive compliance library to accelerate your pharmaceutical compliance journey.

Blog

Stay updated with the latest insights on pharmaceutical compliance, AI governance, and regulatory intelligence.

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AI Governance in Pharmaceutical R&D

Best practices for implementing AI governance frameworks in pharmaceutical research and development.

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Minimal Technical Debt Compliance

How to build compliance infrastructure that scales without accumulating technical debt.

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48-Hour Compliance Assessments

Learn how rapid compliance assessments can accelerate your go-to-market timeline.

Case Studies

Real-world examples of how pharmaceutical companies are transforming compliance with tfives.

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Top 10 Pharma: Up to 1% Faster Label Expansions

How a leading pharmaceutical company accelerated label expansion approvals by 40% using integrated compliance solutions.

  • Minimal post-market failures
  • Up to 40% faster label expansion timeline
  • Integrated lifecycle compliance
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Biotech Startup: First-Time Approval Success

A biotech startup achieved industry-leading first-time approval rate with comprehensive compliance validation from discovery to launch.

  • Industry-leading first-time approval rate
  • Zero data integrity queries
  • Simultaneous global approvals

Whitepapers

In-depth guides and research on pharmaceutical compliance best practices.

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The Compliance Operating System: A New Paradigm

How integrated compliance platforms are transforming pharmaceutical operations from discovery through lifecycle management.

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AI Governance in Pharmaceutical Innovation

Comprehensive guide to implementing AI governance frameworks that meet FDA, EMA, and ICH requirements.

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Minimal Technical Debt Compliance Architecture

Building compliance infrastructure that scales without accumulating technical debt or maintenance burden.

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Multi-Jurisdictional Regulatory Intelligence

Strategies for managing compliance across FDA, EMA, PMDA, and other global regulatory bodies.

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Webinars

Join our live and on-demand webinars to learn from compliance experts.

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48-Hour Compliance Assessments

Learn how rapid compliance assessments can accelerate your go-to-market timeline.

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AI Model Validation Best Practices

Best practices for validating AI models in pharmaceutical research and development.

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Compliance Journey: Discovery to Launch+

Comprehensive overview of compliance requirements across the entire pharmaceutical product lifecycle.

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API Documentation

Integrate tfives compliance capabilities into your systems with our comprehensive API documentation.

Compliance Library

Comprehensive collection of regulatory guidelines, standards, and compliance resources.

Regulatory Guidelines

  • • FDA Guidance Documents
  • • EMA Guidelines
  • • ICH Guidelines
  • • PMDA Requirements

Standards & Frameworks

  • • GxP Standards
  • • ISO 13485
  • • 21 CFR Part 11
  • • HIPAA/GDPR

Best Practices

  • • Data Integrity
  • • Risk Management
  • • Validation Protocols
  • • Audit Preparation

Need Help Finding Resources?

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