Saturday, January 5, 2008

Package development considerations


Package design and development are often thought of as an integral part of the new product development process. Alternatively, development of a package (or component) can be a separate process, but must be linked closely with the product to be packaged. Package design starts with the identification of all the requirements: structural design, marketing, shelf life, quality assurance, logistics, legal, regulatory, graphic design, end-use, environmental, etc. The design criteria, time targets, resources, and cost constraints need to be established and agreed upon.

Transport packaging needs to be matched to its logistics system. Packages designed for controlled shipments of uniform pallet loads may not be suited to mixed shipments with express carriers.
An example of how package design is affected by other factors is the relationship to logistics. When the distribution system includes individual shipments by a small parcel carrier, the sortation, handling, and mixed stacking make severe demands on the strength and protective ability of the transport package. If the logistics system is for uniform pallet loads that are unitized, the structural design of the package can be designed to those specific needs: vertical stacking, perhaps for a longer time frame. A package designed for one mode of shipment may not be suited for another.
Package design may take place within a company or with various degrees of external packaging engineering. Some sort of formal Project planning and Project Management methodology is required for all but the simplest package design and development programs.

Package development involves considerations for sustainability, environmental responsibiity, and applicable environmental and recycling regulations. It may involve a life cycle assessment which considers the material and energy inputs and outputs to the package, the packaged product (contents), the packaging process, the logistics system, waste management, etc. It is necessary to know the relevant regulatory requirements for point of manufacture, sale, and use.
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2 comments:

Nocatster said...

This posting would be of interest to your readers from a post atDDL ISTA’s first annual International Transport Packaging Forum. a guest post from Mike Woletz sharing his thoughts on the first annual International Transport Packaging Forum. It would be worth checking out

Nocatster said...

More news, DDL West Technical Director Karen Greene present The Compliance Sweet Spot ? Outlining key activities designed to ensure those in the medical device package testing industry discover the perfect balance between packaging compliance and competitive time to market.