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

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://bit.ly/1Mca4uD

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 [email protected].