Setting Up an Environmental Monitoring Program for Non-Sterile Manufacturing

This webinar will focus on the process of establishing an environmental monitoring program for non-sterile manufacturing facility and the need to design a system and routine that will satisfy the expectations of the global regulatory agencies. 

Why Should You Attend:

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

What exactly is needed to generate a sensible, practicable and reliable program for a non-sterile manufacturing process?

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

Who Will Benefit:

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

QA/QC personnel

Validation specialists

Manufacturing personnel involved in validations

Environmental monitoring specialists

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. Prior to starting his Consulting career, Steve worked for Wallace Laboratories, Inc. as the group leader of medical diagnostics-infectious diseases, Bristol-Myers Squibb bacteriology, managed the Microbiology department at PACO pharmaceutical ( a CMO) and managed quality operations for antibiotic manufacturers and clinical supplies. 

Note:

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

For Registration:

http://www.complianceonline.com/environmental-monitoring-program-for-non-sterile-manufacturing-webinar-training-703444-prdw?channel=sciencedz