THIS TRAINING ON ESTABLISHING CONTROL OF YOUR CLEA 2015 - Gaining and Re-Establishing Control of Your Cleanroom

Website http://bit.ly/1sNxK5s | Edit Freely

Category FDA GXP Compliance - Pharmaceuticals;

Deadline: January 09, 2015 | Date: January 09, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2014-12-19 16:38:04 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

This webinar will focus on starting up a new cleanroom operation covering everything from utilities to environmental monitoring. Routine cleaning and disinfection will also be addressed. Addressing contamination and bringing up the cleanroom after a worst case event will be discussed.

Who Will Benefit:

This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the pharmaceutical, biotech, and medical device fields. The employees who will benefit include:

QA and QC managers

Disinfectant validation managers

Operations managers

Cleanroom managers

Personnel and contractors that clean and disinfect cleanrooms