Terminal Sterilization of Parenteral Drugs

Reliable Industrial Scale Sterilization of Packaged Parenteral Products

GMP regulations require that if a drug product can be sterilized after packaging (without affecting the product quality), it must be. This statement has two significant implications: (a) packaged (liquid) drugs are bulky and heavy, and (b) processing must be effective but also gentle to eliminate the risk of damage to the packaging integrity. Steelco offers a range of equipment to meet these criteria and provide optimized processing with maximum operational efficiency.