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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).

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.

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