Ditch the Spreadsheets, Dive into Efficiency.

Seamlessly integrate QbD principles and risk management practices into your pharmaceutical development process.

ValGenesis iRisk replaces outdated spreadsheets with a purpose-built digital risk management platform that enhances process efficiency and fosters real-time oversight and knowledge sharing. 

Unleash efficiency with:

  • A single, secure repository to consolidate all your QbD data. No more wading through a sea of spreadsheets or worrying about data integrity issues.
  • Seamless data flow across all stages of development, fostering continuity and informed decision-making. 
  • Built-in intelligence to identify potential risks proactively based on predefined criteria and historical data.
  • Reusable assessments to save time and resources.
Ditch the limitations of spreadsheets and embrace streamlined drug development with ValGenesis iRisk. 

Benefits this Solution Provides

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Enhanced Regulatory Compliance

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Accelerated Development Timelines

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Improved Knowledge Sharing

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One-click Reporting

Learn More About QbD Process

Blog Post
How Integrating Risk Assessment and CPV Increases Patient Safety

Integrating risk assessment and continued process verification with digital technology enhances patient safety and optimizes processes in the pharma industry.

Read the Blog Post
Industry Insight
Risk Management Processes for Cell and Gene Therapies

Read the Industry Insight
Industry Insight
A Roadmap for Implementing Analytical QbD

Read the Industry Insight

Talk to us to see how ValGenesis can support your QbD process.