Location: Online

When: October 26, 2018

Time: 10:00 - 11:00 AM

Why you should attend: 

To understand how to develop an adequate risk-based assessment for contamination control and sterility maintenance to ensure compliance with international regulatory guidelines. Also, to understand what Draft Annex 1 requirements are considered arbitrary vs. imposed.

Topics covered: 

  • The draft Annex 1 requirements and their impact on the global manufacturer
  • Technology such as cleaning and disinfection, sterilization and including utilities microbial contamination control program
  • How to develop adequate risk-based assessment to support a harmonized process for contamination control
  • Sterility maintenance to ensure compliance with international regulatory guidelines
  • Draft annex 1 requirements that are considered arbitrary


Register Now.