Several organizations require FDA approved O-rings to be used in their applications. The FDA (Food and Drug Administration) maintains a tight control of the components used in food processing, pharmaceutical, and allied industries.
It also keeps a check on the products being manufactured. It provides a guideline of the components to be used and the standards to be followed when manufacturing or packaging food, beverages, and pharmaceutical products.
Why Use FDA Approved O-Rings in in F&B & Pharmaceutical Industries ?
Before launching a new drug, several tests are conducted to validate the safe consumption of the drug. Similarly, the FDA conducts several tests on the safety and reliability of components like seals and O-rings. These tests ensure that the components can be safely used in F&B and pharmaceutical industries. Two of the most important reasons are:
O-rings form critical components in machines used for manufacturing and packaging food, beverages, and drugs. Over time, the material of the O-ring will leak into the product being manufactured. Hence, it is important to ensure that the material used to manufacture the O-ring is safe.
The reliability of the application greatly depends on the durability of the O-ring. The FDA O-ring should be manufactured such that it can support the application and its operation. If the O-ring is sturdy, it will keep unexpected failures and resultant downtime to a minimum.
Organizations strictly adhere to the FDA standards and guidelines. The products and materials to be used by the FDA help prevent contamination, and ensure reliability and traceability. Some organizations may adopt these systems simply for certification purposes. Irrespective of the intention, the outcome is the production and supply of safe products.
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