Location: Webinar

Validation of VHP® LTS-V Low Temperature Terminal Surface Sterilization Process & Equipment
Thursday, February 14, 2019
10:00 - 11:00 AM EST

Why You Should Attend:

This webinar will help you understand how to evaluate which low temperature sterilization process is the most appropriate and beneficial for your product and manufacturing chain. Additionally, it is important to understand the main requirements of implementing the VHP low temperature terminal sterilization process through validation pre-requisites and requirements.

What We Will Be Covering:

  • An overview of VHP low temperature sterilization technology and applications
  • Different manufacturing scenarios
  • How, when and what to prepare for in terms of implementing VHP sterilization equipment
  • Validation of the sterilization process

Who Will Benefit:

  • Drug and Delivery Device Developers
  • Pharmaceutical and Medical Device Business Developers
  • Aseptic Manufacturing Facility Leaders
  • Validation Managers
  • Packaging CMO Facilities Management
  • Sterility Assurance Department
  • Pharmaceutical Manufacturing Technology Executives and Decision Makers
  • Manufacturers of Implant and Implanted Electronic Devices

REGISTER NOW