White Papers

  1. 5 Ways To Minimize Risks While Preparing Artwork For Carton Packaging
    10/2/2018

    The process of preparing artwork is essential for box packaging. There is a considerable amount of detail that goes into preparation, but it doesn’t have to be a frustrating ordeal.

  2. Performance Validation, Verification, Monitoring and Testing
    9/25/2018

    This white paper gives guidance on the essential processes of validation, verification, and routine performance monitoring for in-line product inspection equipment in food making facilities.

  3. Label Mix-Up Prevention: Using Vision To Improve The Labeling Process
    9/25/2018

    This white paper explains how vision inspection systems help prevent recalls and protect brand reputations.

  4. Maximize Global Regulatory Collaboration In The Marketing Of Combination Products
    9/13/2018

    Combination products in the medical device industry now occupy a substantial market segment. This article focuses on the maximization of global regulatory collaboration in the marketing of combination products.

  5. Human Factors Considerations For Combination Products
    9/12/2018

    For medical devices, the use of human factors and usability engineering (e.g., applying the knowledge of human behavior, abilities, and limitations to the design of a medical device) plays a key role.

  6. Containment: Top Industry Methods And Challenges
    9/12/2018

    Which methods are most prominent in the pharmaceutical containment industry today and what key challenges are pharmaceutical businesses facing.

  7. Considerations In HPAPI Containment Testing
    9/10/2018

    The global HPAPI market was valued at US$14.4 billion in 2016 and is expected to grow at a CAGR of 10.3 per cent, reaching US$34.8 billion by 2025.

  8. Viscous Products No Match For New Container Closure Integrity Technology
    9/5/2018

    New product types and packaging configurations, such as highly viscous formulations, pose a threat to traditional leak-testing methods, challenging current practices for container closure integrity testing. 

  9. Sustainability By Design
    8/23/2018

    Sustainability means a balancing act and the ability to maintain a certain regulatory standard and the approach of in-built sustainability is essential when designing biopharmaceutical facilities.

  10. Engineering For Sterile Product Manufacturing Facilities
    8/23/2018

    This article provides an overview of the regulatory guidelines and the fundamental GMP requirements with regards sterile manufacturing of medicinal products, with a particular focus on engineering aspects.