Darryl Michel Sullivan - Comment

Document ID: FDA-2011-N-0238-0055
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: December 15 2011, at 12:00 AM Eastern Standard Time
Date Posted: January 11 2012, at 12:00 AM Eastern Standard Time
Comment Start Date: November 1 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: December 20 2011, at 11:59 PM Eastern Standard Time
Tracking Number: 80f83587
View Document:  View as format xml

View Comment

Covance would like to ensure that FDA makes sound decisions based on testing data from qualified laboratories. Both FDA and private laboratories must be accredited and must follow good laboratory practices in their testing programs. It is critical that testing be conducted in all situations where detention of food is being considered. The testing must be conducted using validated testing methods that have been accredited and approved. We hope that FDA will issue guidance rules on the approval process for all testing laboratories, so that the laboratory test data can be used for critical situations. We expect that FDA will follow some International standard like ISO 17025 in their rule on lab accreditation. It is important that the rule contain details about the lab qualification. We would like to understand how the Fee Provisions will affect the contract testing laboratories and if there will be any fees associated with becoming certified as a third party testing lab under FDA FSMA.

Related Comments

    View All
Total: 11
Anonymous - Comment
Public Submission    Posted: 11/15/2011     ID: FDA-2011-N-0238-0053

Dec 20,2011 11:59 PM ET
Darryl Michel Sullivan - Comment
Public Submission    Posted: 01/11/2012     ID: FDA-2011-N-0238-0055

Dec 20,2011 11:59 PM ET
Canadian Horticultural Council - Comment
Public Submission    Posted: 01/11/2012     ID: FDA-2011-N-0238-0056

Dec 20,2011 11:59 PM ET
International Warehouse Logistics Association (IWLA) - Comment
Public Submission    Posted: 01/11/2012     ID: FDA-2011-N-0238-0057

Dec 20,2011 11:59 PM ET
Paul W Hostetter - Comment
Public Submission    Posted: 01/11/2012     ID: FDA-2011-N-0238-0058

Dec 20,2011 11:59 PM ET