White Papers

  1. Executive ERP Evaluation And Investment Roadmap For Food/Beverage Manufacturers

    A guide to help you toward the reason and value for making a change and align your organization on the specific benefits of a new software solution across all of your operations and supply chain.

  2. How To Guarantee All-Round Glass Inspection

    Glass is frequently the preferred packaging material for food and pharmaceutical manufacturers. However, checking for foreign bodies in a finished pack is critical, as just one shard could have catastrophic consequences.

  3. Performance Validation, Verification, Monitoring and Testing

    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.

  4. The Principles of Due Diligence For Quality Control and Legal Defense

    The white paper explains the importance of identifying foreign body contaminants in food and can be used as a checklist to evaluate the various metal detectors and x-ray inspection systems on the market.

  5. Understanding Food Label Regulations Of The U.S., EU, And China

    There are an increasing number of ways in which a label might now fail to meet one of those specifications, making a strict label quality control process more necessary than ever.

  6. Label Mix-Up Prevention: Using Vision To Improve The Labeling Process

    This white paper explains how vision inspection systems can help protect consumers and your brand.

  7. Tips For Cleaning And Sanitizing Pneumatic Conveying Lines

    Pneumatic conveying is an effective form of moving dry materials in food manufacturing. However, the long lengths of conveying pipe present challenges in terms of addressing cleanliness and sanitation.

  8. How To Select A Feeder For Your Process = Understanding Your Bulk Material

    Selecting a feeder for solid material at the correct processing rate means understanding materials and flow. This article describes common feeders and how to match a feeder to your material's flow behavior.

  9. Sustainability By Design

    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

    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.