Throughout the manufacture of pharmaceutical products, both non-sterile and sterile products are susceptible to the microorganisms they contact during the manufacturing process.  This Pharma webinar will equip attendees with the tools they need to meet the challenge.

Learning Benefits

• Learn how to Develop a Cleaning and Disinfection Program 
• Determine the Implementation Aspects of a Cleaning and Disinfection Program 
• Monitoring and Interpretation of the Results of the Cleaning and Disinfection Program
• Understand Resistance and Rotation of Disinfectants and Its Meaning to the Facilities 
• The Use of USP<1072>, <1227> and <51> within the Development of Disinfectant Efficacy Programs 
• A Review of Case Studies and Selected Warning Letters