CIP or clean-in-place holds immense significance in the pharmaceutical industry, regardless of the setup, be it a drug manufacturing plant, laboratory, or any other pharma operations. The primary focus is on effectively cleaning and sterilizing the equipment on a regular basis to ensure zero contamination and risk of product quality, thereby ensuring that it is safe for patients to consume. Implementing CIP also saves time, as disassembling and assembling the equipment is no longer required for cleaning purposes. However, the incorporation of CIP systems during the design phase of a facility still needs to gain priority to ensure that the cleaning process is seamless and efficient. By doing so, pharmaceutical companies can significantly reduce the risk of contamination, cutting the cost of cleaning, and enhancing the overall quality of the product.