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Packaging Automation Overview

The automation of any packaging process is dependent on the product’s attributes, production parameters and goals, and how products are delivered to and from packaging equipment. This paper provides a high-level overview of key considerations of packaging automation.

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Regulatory Considerations for the Medical Industry

Healthcare costs have skyrocketed, making packaging of volume-driven Class I and Class II medical devices such as syringes, intravenous (IV) administration kits and catheters, a target for cost and risk containment. Packaging helps ensure devices are delivered contaminant-free, safe to use, and able to withstand a wide range of shipping and storage conditions. While packaging and sterilization are mostly technologies that rely on proven methods, the emergence of smaller, more complex devices and kits combined with cutting-edge barrier materials and flexible films is challenging the status quo of legacy packaging solutions.

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Digital Transformation for the Medical Device Industry

Medical Device Packaging and Digital Transformation Whitepaper The convergence of the physical and digital worlds is impacting every aspect of our society, and Medical Device Manufacturing is no exception. This “digital transformation” has pushed the boundaries of what is possible. In the past, industrial environments have been slow to evolve technologically due to complexity and…

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Automation Justification for Medical Device Packaging

What not to overlook when justifying medical device packaging automation. An insider’s guide on building your best business case for packaging automation – How to gain executive support and approval of your next big-ticket packaging automation investment by addressing qualitative and quantitative justifications. Click here to access this paper.

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