To maintain safety and quality of parenteral preparation, Ziska has developed the cGMP compliant processes and machinery as well as the validated source of Raw material and excipients and their compliant testing facility to ensure purity and potency. Next, these materials undergo precise measurements and mixing in a controlled environment to create the formulation. The mixture is then subjected to sterilization processes, such as filtration or heat treatment, to eliminate any potential contaminants. Afterward, the product is filled into appropriate containers, sealed, and labeled, adhering to strict regulatory guidelines. Throughout the entire manufacturing process, stringent quality control measures are implemented to maintain the integrity of the parental product.