World Packaging Day

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Across
  1. 3. The complex network and processes involved in the movement of goods from origin to the intended end-user, encompassing various environmental and handling hazards.
  2. 4. Predictive study using intensified conditions over less time.
  3. 6. Regulation required for medical devices / nickname of a team member
  4. 8. An abrupt and transient mechanical stimulus that can impart significant energy to a packaged product, potentially causing damage.
  5. 9. The point at which a package or material catastrophically fails under internal or external pressure, indicating its strength limitations.
  6. 11. A physical, chemical, or biological device that provides a measurable or observable output confirming that a specific parameter or condition has been achieved within a defined tolerance.
  7. 15. The inherent ability of a packaging system to absorb shocks, vibrations, and other stresses without compromising its primary functions.
  8. 16. Ability of a package to return to its original shape after deformation.
  9. 17. The quantifiable remnants of a substance or energy remaining on a device post-processing, impacting its safety or efficacy.
  10. 19. Pertaining to the final stage or condition, often for sterilization, critical in assessing the ultimate state of a packaged product.
  11. 20. A meticulously designed series of controlled tests replicating real-world stresses to evaluate package robustness.
  12. 21. Transmission rate of substances through packaging.
  13. 23. Potential weaknesses in the journey of packaged goods.
  14. 24. A series of validated procedures undertaken to render a used medical device safe and effective for its intended subsequent use.
  15. 25. Process of removing or deactivating harmful microorganisms.
  16. 27. The unimpaired condition of a package, ensuring the maintenance of its protective and barrier functions throughout the supply chain.
  17. 28. Specified range of acceptable values for a package attribute.
  18. 29. The state of being free from viable microorganisms, a critical attribute maintained by the sterile barrier system.
Down
  1. 1. Measure of a material's resistance to breaking under tension.
  2. 2. Process of verifying measurement equipment accuracy.
  3. 5. Enclosure designed to contain, protect, market, and ultimately add value to a product throughout its lifecycle.
  4. 6. Resistance of a material to scratching or abrasion.
  5. 7. Absence of pyrogenic substances in the final product.
  6. 10. Gradual decline in package or product quality over time.
  7. 12. The documented ability of a package to meet predefined functional requirements under specified and often challenging conditions.
  8. 13. Level of confidence in a measurement or test result.
  9. 14. The process of consolidating individual packages into a larger, more stable load for efficient handling and transport.
  10. 18. The period of time during which a packaged product is expected to remain acceptable for its intended use under specified storage conditions.
  11. 22. Establishing documented evidence that provides a high degree of assurance that a specific process will consistently produce a product meeting its pre-determined specifications and quality attributes.
  12. 25. The hermetic or non-hermetic junction formed by bringing together one or more packaging components to maintain barrier properties.
  13. 26. The ability to follow the history, application, location, and movement of a product and its components through all stages of the supply chain.