The design of cleanroom products is an important and necessary process in many industries, including medical, food and electronics. These sectors require particularly clean and controlled conditions to ensure product quality, safety and performance in compliance with GMP and FDA requirements. There are several key aspects to consider when designing cleanroom products. Here are some of the most important ones.
First, the purity classification sets the basis for the design process. The purity classification describes the cleanliness of the air in the cleanroom for specific particle sizes. The purity class determines the level of filtration required and can vary depending on the industry. When designing, it is important to understand the purity class requirements and ensure that the products designed meet these requirements.
Secondly, material choice plays an important role in the design of cleanroom products. It is important to choose materials that are compatible with clean environments and that do not release pollutants or particles into the surrounding air or product. For example, stainless steel and certain polymers are common material choices because they are durable, do not shed particles and are easy to clean.
Thirdly, the design must pay attention to the cleanability and ease of use of the products. Their structures must also not hinder cleaning or be particularly susceptible to collecting dirt. Easy-to-clean and maintain cleanroom products are efficient to use and maintain. In terms of ease of use, it is important to take into account the clothing required in the cleanroom. For example, the user of a tool may have several gloves on, which has a significant impact on dexterity.
By taking these three basic principles into account, it is possible to design very high quality products for cleanrooms. At Hefmec, we have solid experience in designing tools and lifting equipment for cleanroom environments. For examples and more information, visit our Cleanroom products page. We also supply cleanroom products designed to meet GMP and FDA requirements.
Written by Mika Julin, Project Engineer, Account Manager – Pharmaceutical Industry
