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

ICR 202106-0910-009

OMB: 0910-0887

Federal Form Document

Forms and Documents
Document
Name
Status
Justification for No Material/Nonsubstantive Change
2021-06-16
Supplementary Document
2020-05-05
Supporting Statement B
2020-01-13
Supporting Statement A
2021-06-16
ICR Details
0910-0887 202106-0910-009
Received in OIRA 202001-0910-003
HHS/FDA CTP
Center for Tobacco Products, Food and Drug Administration Funded Trainee/Scholar Survey
No material or nonsubstantive change to a currently approved collection   No
Regular 06/16/2021
  Requested Previously Approved
05/31/2023 05/31/2023
2,524 2,524
143 143
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
Follow-Up Email
Informed Consent
Lead Letter
Notification Email
Survey
Trainee List Email

  Total Request 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 2,524 0 0 0 0
Annual Time Burden (Hours) 143 143 0 0 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No
This is a new information collection.

$76,150
Yes Part B of Supporting Statement
    Yes
    No
No
No
No
No
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.
06/16/2021


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