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  • …  
    • Home
    • About 
      • Who We Are
      • Our Team
    • Services 
      • QMS
      • Project Management
      • Inspection Remediation
      • Validation and Qualification
      • Cannabis
      • Auditing
      • Implementation of AI
      • Professional Training
      • CMC Development
    • Events & Conferences
    • Contact Us
    • Publications 
      • Cybersecurity of Medical Device
      • The AI Act

     

     

    • Home
    • About 
      • Who We Are
      • Our Team
    • Services 
      • QMS
      • Project Management
      • Inspection Remediation
      • Validation and Qualification
      • Cannabis
      • Auditing
      • Implementation of AI
      • Professional Training
      • CMC Development
    • Events & Conferences
    • Contact Us
    • Publications 
      • Cybersecurity of Medical Device
      • The AI Act
    • …  
      • Home
      • About 
        • Who We Are
        • Our Team
      • Services 
        • QMS
        • Project Management
        • Inspection Remediation
        • Validation and Qualification
        • Cannabis
        • Auditing
        • Implementation of AI
        • Professional Training
        • CMC Development
      • Events & Conferences
      • Contact Us
      • Publications 
        • Cybersecurity of Medical Device
        • The AI Act
      • Validation and Qualification

        We can help you successfully develop and execute validation projects from start to finish for you various needs.

      • With two decades of validation experience, the team at YS Consulting can help you successfully develop and execute validation projects from start to finish for you various needs: Equipment and System Validation (e.g. HVAC, cleanrooms, water system, machinery, autoclaves etc.), Process Validation, Cleaning Validation and Computer System Validation (CSV).

        Our services include validation planning and initiation, validation project management, as well as remediation, optimization, and deviation handling.

        We can support you in creating and reviewing validation documents such as Validation Master Plan (VMP), User Specification Requirements (URS), Design Qualification (DQ), Factory Acceptance Test (FAT), Site Acceptance Test (SAT), Installation Qualification (IQ), Operational Qualification (OQ) and performance Qualification (PQ) protocols and reports.

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      Canada: +1-514-571 6844

      USA: +1-617-960-6818

      France: +33-745-67-53-87

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