Ensuring an Effective Design of Cleanroom and Facility Validation Compliant with FDA Regulations

MessageThis Webinar is over
Date Oct 21, 2015
Time 03:00 PM EDT
Cost $227.00

Product Format: Live Audio conference
Presenter(s): Dr. David Lim, Ph.D., RAC, ASQ-CQA
Conference Date: Wed, Oct 21, 2015
Aired Time: 1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length: 60 minutes
Price: $2227
This audio conference by expert speaker Dr. David Lim is intended to discuss FDA regulations and the requirements for an effective cleanroom and facility validation as part of current good manufacturing practices (CGMP) for sterile drug and biological products. This session will greatly help you understand and establish an effective environmental monitoring program in view of CGMP (USP, ISO and FDA recommendations). 
For more information, visit http://www.audioeducator.com/pharma-biotech/effective-cleanroom-design-and-validation-10-21-2015.html
Special Offer: Use code SAVE10 to get 10% discount.
Not able to attend the audio session? We will provide you with a replay of the session, or you can request a DVD recording.
For any queries feel free to contact Adam K at 1-866-458-2965 or e-mail Adam at customerservice@audioeducator.com.


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