Biopharmaceutical Raw Materials & Viral Safety for Biologicals 2015

Topics

• Filtration techniques including nanofiltration, with feedback direct from suppliers and manufacturers
• Next generation sequencing and emerging detection technologies
• How to implement QbD in your design space, with feedback direct from the regulators
• Methods for carrying out successful risk assessment
• Global regulatory requirements
• The interpretation of viral safety data from next generation techniques
• Emerging viral threats including Hepatitis E and Vesivirus

Who should Attend

• Heads of Marketing and Business development
• Quality controllers & Quality assurance managers
• Head of Regulatory
• Scientists
• Procurement directors