Center for Tobacco Products, Food and Drug Administration Funded Trainee/Scholar Survey

ICR 202001-0910-003

OMB: 0910-0887

Federal Form Document

ICR Details
0910-0887 202001-0910-003
Active
HHS/FDA CTP
Center for Tobacco Products, Food and Drug Administration Funded Trainee/Scholar Survey
New collection (Request for a new OMB Control Number)   No
Regular
Approved with change 05/06/2020
Retrieve Notice of Action (NOA) 01/13/2020
  Inventory as of this Action Requested Previously Approved
05/31/2023 36 Months From Approved
2,524 0 0
143 0 0
0 0 0

The U.S. Food and Drug Administration’s (FDA) Center for Tobacco Products (CTP) and the National Institutes of Health (NIH) maintain an interagency partnership to foster the development of the emerging field of tobacco regulatory science (TRS). This study will use the Center for Tobacco Products, Food and Drug Administration Funded Trainee/Scholar Survey to gather data on the characteristics, activities, and impact of training programs funded by the CTP and other partners. This evaluation will also determine how CTP-funded research and associated training programs and activities increase knowledge and skills related to TRS and interest to pursue careers in a TRS-related field. This survey provides support to determine the extent to which programs and activities generate positive impacts to increase the number of researchers who focus on TRS and TRS-related topics, specifically within CTP’s priority domains. The survey builds upon previous evaluations of trainees and training activities and provides necessary evidence to inform FDA decision-making. The web survey will gather responses from current and former Tobacco Centers of Regulatory Science (TCORS) trainees and other CTP-funded trainees and scholars. Results will provide insights and directions to support future training and funding investments.

None
None

Not associated with rulemaking

  84 FR 48148 09/12/2019
85 FR 713 01/07/2020
No

7
IC Title Form No. Form Name
Email Invitation
Survey
Follow-Up Email
Trainee List Email
Notification Email
Informed Consent
Lead Letter

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 2,524 0 0 2,524 0 0
Annual Time Burden (Hours) 143 0 0 143 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
This is a new information collection.

$76,150
Yes Part B of Supporting Statement
    Yes
    No
No
No
No
Uncollected
Ila Mizrachi 301 796-7726 ila.mizrachi@fda.hhs.gov

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
01/13/2020


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