Mesa Labs Articles

  1. Ensure Safety And Compliance With A Guide To Sterilization Validation 5/28/2025

    Sterilization validation is vital in pharma and medical device manufacturing to ensure product safety and regulatory compliance. Explore essential principles, best practices, and frameworks for effective implementation.

  2. Specific Sterilization Method: Best Practices And Common Pitfalls 5/28/2025

    Validating sterilization methods like steam, VH₂O₂, and EO is essential for safety and compliance. Learn best practices, avoid common pitfalls, and optimize your validation strategy effectively.

  3. What Is A Bowie-Dick Test And Why Is It Important? 5/28/2025

    Effective sterilization is vital in pharma and medical device manufacturing. Discover how the Bowie-Dick test ensures vacuum sterilizer performance, safeguards patient safety, and strengthens your sterility assurance program.

  4. Understanding D-values: A Simplified Explanation For Busy Professionals 5/28/2025

    D-values are essential for ensuring sterility in pharma and medical device manufacturing. Explore a simplified concept that helps professionals optimize sterilization processes and ensure product safety with confidence.

  5. Top 3 Mistakes Companies Make During Sterilization Validation 5/27/2025

    Sterilization validation is essential for product safety and compliance. Discover the top three mistakes companies make and learn practical strategies to avoid delays, non-compliance, and patient safety risks.

  6. The Ultimate Guide To Biological Indicators 5/27/2025

    Discover why biological indicators are the gold standard for sterilization validation in pharmaceutical and medical device manufacturing, as well as how choosing the right one ensures safety, compliance, and product integrity.

  7. 5 Biggest Sterilization Challenges Facing Manufacturers 5/27/2025

    Sterility is non-negotiable in pharmaceutical and medical device manufacturing. Discover the top five sterilization challenges facing manufacturers today and the proven strategies to overcome them while ensuring compliance and safety.

  8. Why Perform A D-Value Study? Reference Review 10/31/2024

    Understanding how a product influences microorganisms' resistance is crucial. Read about relevant standards and references as well as recommendations for performing product D-value studies.

  9. Reducing Risks In Your SIP Validation Cycles 8/6/2024

    Utilizing tape for positioning during Sterilize in Place (SIP) validation can introduce numerous issues. Explore the top eight reasons why tape should be avoided during SIP validation cycles.

  10. How To Prove A Sterility Assurance Level Of 10⁻⁶ 2/13/2024

    Explore the Biological Indicator/Bioburden (BI/BB) method for achieving sterilization of products along with the prerequisite studies needed to develop the sterilization process.