eLaws | eCases | United States Code | Federal Courts |
Home » Rulemaking » Jim Tozzi (Center for Regulatory Effectiveness) - Testimony

Jim Tozzi (Center for Regulatory Effectiveness) - Testimony

Document ID: FDA-2011-N-0443-0006
Document Type: Public Submission
Agency: Food And Drug Administration
Received Date: August 25 2011, at 12:00 AM Eastern Daylight Time
Date Posted: September 28 2011, at 12:00 AM Eastern Standard Time
Comment Start Date: June 22 2011, at 12:00 AM Eastern Standard Time
Comment Due Date: September 23 2011, at 11:59 PM Eastern Standard Time
Tracking Number: 80ef181d
View Document:  View as format xml

View Comment

Attached are the Center for Regulatory Effectiveness' comments on FDA's Scientific Evaluation of Modified Risk Tobacco Product Applications proceeding.

Attachments:

Jim Tozzi (Center for Regulatory Effectiveness) - Testimony, CRE.ModifiedRisk-Testimony

Title:
Jim Tozzi (Center for Regulatory Effectiveness) - Testimony, CRE.ModifiedRisk-Testimony

View Attachment: View as format pdf

Related Comments

    View All
Total: 56
American Cancer Society (ACS), Cancer Action Network (CAN), American Heart Association (AHA), American Lung Association (ALA), Campaign for Tobacco-Free Kids (TFK), American Public Health Association (APHA) - Comment
Public Submission    Posted: 09/23/2011     ID: FDA-2011-N-0443-0003

Sep 23,2011 11:59 PM ET
Jim Tozzi (Center for Regulatory Effectiveness) - Testimony
Public Submission    Posted: 09/28/2011     ID: FDA-2011-N-0443-0006

Sep 23,2011 11:59 PM ET
Gilbert Ross M.D. - Testimony
Public Submission    Posted: 09/28/2011     ID: FDA-2011-N-0443-0007

Sep 23,2011 11:59 PM ET
Patrick Johnson - Comment
Public Submission    Posted: 09/28/2011     ID: FDA-2011-N-0443-0008

Sep 23,2011 11:59 PM ET
Leena Bhola - Comment
Public Submission    Posted: 09/28/2011     ID: FDA-2011-N-0443-0009

Sep 23,2011 11:59 PM ET