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Wednesday, March 11, 2015
1:00 PM - 2:00 PM
1:00 PM - 2:00 PM See all dates and Times
http://www.audioeducator.com/pharma-biotech/combination-drug-products-cgmp-03-12-2015.html?utm_campaign=AEVENTS
Product Format: Live Audio Conference Presenter(s): Dr. David Lim, Ph.D., RAC, ASQ-CQA Conference Date: Thu, Mar 12, 2015 Aired Time: 1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length: 90 minutes
Price: $227
Join expert speaker Dr. David Lim, Ph.D., RAC, ASQ-CQA to discuss US FDA Final Rule for current Good Manufacturing Practice (cGMP) for combination products and how firms can achieve compliance with quality system regulations as well as compliance with drug cGMP requirements for combination products. He will discuss cGMP Requirements for a Co-Packaged or Single entity Combination Product; how to implement Compliance with Biological Product and HCT/P Requirements and have a comparative discussion on 21 CFR Parts 210/211, 600-680, 820, and 1271.
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.
Length: 90 minutes
Price: $227
Join expert speaker Dr. David Lim, Ph.D., RAC, ASQ-CQA to discuss US FDA Final Rule for current Good Manufacturing Practice (cGMP) for combination products and how firms can achieve compliance with quality system regulations as well as compliance with drug cGMP requirements for combination products. He will discuss cGMP Requirements for a Co-Packaged or Single entity Combination Product; how to implement Compliance with Biological Product and HCT/P Requirements and have a comparative discussion on 21 CFR Parts 210/211, 600-680, 820, and 1271.
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.
