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Summary of this article

Cleanroom-compatible packaging requires a strategic decision based on the process: will the packaging actually enter the cleanroom, and which classification must it meet? For medical technology, semiconductors, high-tech, defence and other critical sectors, this directly determines the control of contamination, quality and compliance. Cleanroom packaging is therefore not a standalone product specification, but an integral part of the overall flow of goods and processes.

Inadequate packaging can introduce particles, complicate cleaning and lead to rejection, repackaging, production downtime or loss of customer confidence. Overengineering also creates risks, including unnecessarily high material and process costs, longer lead times and additional supply chain complexity. In particular, the transition between the transport environment, airlock and cleanroom requires clearly defined responsibilities and a carefully considered combination of inner and outer packaging.

Faes therefore analyses where the packaging is opened, which standards apply and which requirements arise regarding materials, cleanability, handling and reuse. Based on this analysis, a standard, reusable or cleanroom-compatible solution is selected. This turns packaging management into a strategic tool for structurally reducing contamination risks and improving quality, continuity and operational performance.
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Cleanroom-proof or standard packaging?

Your client processes the components you supply in a cleanroom. Is it therefore necessary for the packaging in which you deliver products to be cleanroom-proof? Or is standard packaging sufficient?

Stroomschema met verpakkingsopties voor cleanroom toepassingen volgens ISO-normen en standaard verpakking voor eenmalig of herbruikbaar gebruik

In the diagram above, we have clearly outlined the deciding factors. The most important question to ask your client is: Will the packaging enter the cleanroom? If the product is removed from its packaging before entering the cleanroom, then the packaging obviously does not need to meet cleanroom standards.

Understanding your client's process

The above probably sounds quite logical, yet it happens that the assumption is made that a package must be cleanroom-proof, when in practice this may not be necessary. A shame, because then you unnecessarily have a special (and expensive) packaging developed, while standard packaging suffices. On the other hand, it can also happen that you do not think about this at all and then it turns out that your packaging does not meet your customer’s requirements.

Understanding the steps of your client’s manufacturing or assembly process is thus essential when creating a set of requirements, as the basis for the final packaging design.

Scenario 1: Packaging does enter the cleanroom

When you know for sure that the packaging does go into the cleanroom, the next question arises: “what must the packaging meet?”. When your client processes or assembles products in a cleanroom, there are bound to be certain parameters determined in terms of the requirements a product must meet and how “clean” it must be.

What exactly are the parameters and does the ISO-5 or -7 standard apply? Do you lack this crucial information or could you use help interpreting and making concrete the package of requirements? At Faes, we know all about cleanroom packaging.

Our packaging experts ask the right questions and proactively think with you about smart, efficient and effective packaging solutions.

What makes a package suitable for the cleanroom or not?

Many standard packaging materials are absolutely unsuitable for use in cleanrooms. Examples include:

  • Packaging with seams and edges where contamination (dirt or dust particles) is likely to occur;
  • Components of packaging made of such materials as; silicones, evaporating plastics, certain greases (lubricants), non-anodized aluminum and ferrous metals;
  • Materials with open structures or pores so that dust cannot accumulate in them;
  • Packaging material made of wood, cardboard or paper, which contains fibers.

Standardization and classification

As the basis for the classification and specification of cleanroom standards, ISO standards apply. In the industries in which Faes operates, the ISO-5 and ISO-7 standards are the most common. The classification and standards describe the maximum number of particles and other contaminants that may be present per defined area, for example per cubic decimeter. For ASML suppliers, the ‘grade 4’ and ‘grade 2’ standards, among others, are important to keep an eye on when making an application. It is also important to ask about these grades when supplying to an ASML partner. Because, while they may overlap with ISO standards, ASML’s standards stand on their own.

Want to know exactly which standards apply to your company or your client? We have detailed for you in this white paper various technical data, specifications, classifications and ISO standardization requirements around clean packaging.

Scenario 2: Packaging does not enter the cleanroom

If the packaging does not have to be cleanroom-proof, that does not mean that there are no other opportunities to optimize your packaging and packaging process. There most certainly are. For example, have you thought about delivering your products in reusable packaging? If you regularly deliver the same components to your customer, reusable packaging is an efficient and sustainable packaging solution. You can calculate exactly how many returns the investment pays off and at the same time how much packaging waste you save.

Do you find this interesting? Then also read fellow packaging expert Corné’s blog on how sustainable packaging helps improve your performance.

Want to know more about cleanroom-proof packaging?

Or do you have another packaging issue where you could use the expertise of a packaging expert? Ask your question in the contact form below and we’ll get back to you quickly. Do you have an urgent question and want to speak directly to me or one of my colleagues? Feel free to call us!

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Robert Verboven

Robert Verboven

Sales Manager

Robert Verboven is Sales Manager at Faes and advises customers on smart packaging solutions within the industry. He translates complex packaging needs into practical solutions that contribute to a more efficient supply chain.

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