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Maintaining the sterility and safety of pharmaceutical products is paramount in the sector. Be it injectable medications or biologics, packaging for storage and transportation needs to be such that it does not allow contamination. Here, a container closure integrity testing kit proves to be important. It assists pharmaceutical firms in ensuring that their packaging is leak-free, tamper-proof, and compliant with rigorous regulatory requirements. By selecting an appropriate kit, companies can ensure the quality of products, safeguard patients, and comply with international regulations. We provide advanced container closure integrity testing kits that ensure product safety, compliance, and peace of mind for pharmaceutical manufacturers.
Why Container Closure Integrity Testing Matters
Container Closure Integrity Testing (CCIT) refers to the process of ensuring a seal in a container actually keeps a product from leaking or contaminating. Whether vials, syringes, ampoules, or bottles, every type of packaging needs to be intact during its usable lifetime. Pharmaceutical products need not be tested if left unguarded, and risk exposure to bacteria, moisture, or air, potentially affecting safety and efficacy. Due to this, regulatory bodies such as the FDA and EMA mandate strict validation of sterile packaging.
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