Package Inspection White Papers & Case Studies

51. Five Steps To Packaging Quality Assurance For Liquid Pharmaceuticals 3/16/2022

    Find solutions to five key challenges of quality assurance and information to help you identify which product inspection products can best support your application.

52. How To Properly Test Your Industrial Metal Detector 2/7/2019

    In this paper, we explain the differences between validation, verification and routine performance monitoring and give an overview of recommended test methods for different metal detection systems.

53. Helium Leak Detection On Plastic Ophthalmic Containers 6/8/2023

    A major pharmaceutical entity wanted to ascertain their container system's seal quality. Explore results from a series of leak testing projects that highlighted key issues with their plastic containers.

54. Container Closure Integrity Testing For Sterile Vial Products In Deep Cold Storage 12/28/2018

    During QC testing, a number of vials of liquid vaccine product stored at -80°C were found to have an overpressure, representing a serious safety risk and they needed to identify the root cause.

55. A Holistic Strategy To Ensure Container Closure Integrity Of Sterile Injectable Vial Product 1/25/2021

    Recent regulatory guidance has triggered changes in industry best practices in the area of container closure integrity testing (CCIT). However, assuring good CCI of sterile injectable product goes beyond CCI testing. A more science-based holistic approach that includes robust design & qualification of the process and the implementation of appropriate process controls is required. This article describes a framework enabling such a holistic approach to CCI that assures both the primary packaging and the process contribute to good CCI of sterile injectable vial product.

56. 2015 – Meeting Serialization Challenges With Time, Resources & Strategy 6/5/2012

    The year 2012 has come to signify “the end of the world” in pop culture, a sentiment fueled by doomsday theorists. Despite scientific fact to the contrary, a feeling of uncertainty and unpreparedness lingers in the minds of the general population.

57. Oxygen Sensitive Product: Comparing Oxygen Testing Methods 3/7/2021

    The accurate determination of oxygen concentration as a critical quality parameter for oxygen-sensitive products is important across the product life cycle activities. Traditional methods for determining headspace oxygen levels in parenteral containers, such as electrochemical methods or gas chromatography, are slow and destructive. This article describes several case studies comparing non-destructive laser-based oxygen headspace analysis with electrochemical oxygen analysis and gas chromatography.

58. Leveraging CDMO Expertise To Achieve Aseptic Fill/Finish Success

    Achieving high-quality drug product requires a combination of meticulous quality control measures, personnel expertise, and judicious application of technology — benefiting patients and the industry.

59. OEE And Product Inspection 2/13/2025

    Explore the calculation of Overall Equipment Effectiveness (OEE) and the impact of product inspection equipment on OEE in the pharmaceutical industry.

60. Avoid Delays From Failed Stabilities Due To Package Integrity - How To Ensure Your Blister Package Passes Stability 4/12/2012
    Pharmaceutical companies all share the same goal: Delivering safe and effective drugs to patients. One aspect of achieving this objective is conducting stability studies that demonstrate to regulatory organizations that a drug’s formulation is safe and effective. By Zuzana Sabova-Kepic, Manager, Barrier Packaging, Analytic Lab and Lead Technical Specialist, Honeywell HealthCare and Packaging