The Microbial Factor of Non-Sterile Cleaning Validation

This webinar will focus on the microbiological element of non-sterile manufacturing cleaning validation and the need to design a robust cleaning routine. It will address the different pharmacopoeia regulations and current regulatory trends. It will also cover the theory in setting the baseline profile and limits along with determination of routine testing.

Why Should You Attend:

All non-sterile pharmaceutical products require some level of microbial control and bioburden testing. A satisfactory cleaning validation must ensure the best chances of consistent satisfactory environmental control.

What exactly is needed to set the guideline for a non-sterile manufacturing environmental monitoring program?

What are the actions your company must consider in controlling a non-sterile environment?

Is your cleaning validation sufficient to support the sanitation schedule of the manufacturing environment?

Who Will Benefit:

This webinar will provide valuable information to all companies that are in need of creating a cleaning validation program for non-sterile manufacture of pharmaceuticals or the improvement, remediation of existing programs.

QA/QC personnel

Validation specialists

Manufacturing personnel involved in validations

Instructor Profile:

Steve Yeger, is owner and President of Steven Yeger Consulting, a consulting firm based in the United States with that has serviced pharmaceutical clients worldwide. 

Note:

Use coupon code 232082 and get 10% off on registration.

For Registration:

http://www.complianceonline.com/microbial-factor-of-non-sterile-cleaning-validation-webinar-training-703360-prdw?channel=sciencedz