Package Inspection White Papers & Case Studies

81. 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.

82. Digital Color Inspection Optimizes Color Management In Packaging 6/5/2018

    Color is one of, if not the most critical component of a brand’s image, but it is also one of the most finicky and subjective components companies need to agree on.

83. How Real-Time Checkweigher Monitoring Boosts Profitability 7/14/2017

    With ingredient costs rising, it’s critical to minimize product give away. This paper discusses advanced checkweighing technology and how it ensures over/under-filled containers don't reach the marketplace.

84. Checkweighers: Using Data To Minimize Expensive Product Giveaways 7/14/2017

    Making sure final product weight is within acceptable min/max ranges is a critical manufacturing objective for F&B companies. This article details how checkweighers help ensure proper fill levels.

85. Medical Device Labeling — Regulations In The U.S., EU, And China 7/13/2017

    While there are a certain amount of commonalities in regulations in each country, there are differences which necessitate care from global manufacturers when distributing products.

86. 5 Steps To Decide What Contaminant Detection Equipment Fits Your Needs 6/7/2016

    Contaminants are a fact of life for food manufacturers, making contaminant detection a necessity.  This five-step process is one way to calculate the payback of purchasing contaminant detection systems.

87. Checkweighing Challenges Call For Customization 2/27/2016

    Checkweighers are key to measuring efficiency and cost of a packaging line. However, there are factors that may require customization that play a role in the success of your checkweigher.

88. Verification Steps To Test Metal Detector Failure 9/24/2015

    Verification is one step to help ensure the food safety system is working to prevent, control or, significantly reduce public health hazards. Verification includes validating the steps to ensure the process will work, and secondly includes the evaluation activities that verify the system continue to work. Verification activities are clearly defined in FSMA and the Preventive Controls Rule, as well as in current regulated HACCP requirements. Here is an example of how to apply the required verification steps — as outlined in the FDA’s proposed Preventive Control rule — to test metal detector failure.

89. Improving Quality Processes For Medical Device Development And Manufacturing 3/21/2013

    Organizations that consistently develop and launch new products efficiently in an environment of increasing regulatory scrutiny, successfully manage regulatory risk. By Mike Kuehne, ACSYS, Inc.

90. Factors To Consider When Selecting A Vision Inspection System For Personal Care Products 3/5/2013

    Implementing a vision inspection solution to monitor the quality and security of your personal care product is an effective quality control method that allows processes to reach maximum throughput and productivity. By Wayne Eide