PDA TRI Aseptic Processing Events

Aseptic Processing is crucial in the drug manufacturing process. This highly regulated area requires that manufacturers are compliant to global regulatory bodies to ensure the production of safe parenteral products. PDA TRI Aseptic Processing events allow participants to share best practices in aseptic processing beyond the commonly known touchpoints. In addition, these events will explore the following various areas via theory and practicum: Sterilization, RABS Systems, Isolators, Regulatory, Risk Assessment, Packaging, Human Factors, Cleaning and Disinfection, Manual and Automated Aseptic Processes.