PTTMS Fast track survey

PTTMS Fast Track_ 2019 updated TL_DW.docx

Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery (NIAID)

PTTMS Fast track survey

OMB: 0925-0668

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Request for Approval under the “Generic Clearance for the Collection of Routine Customer Feedback” (OMB#: 0925-0668 Exp., date: 04/2022)

Shape1 TITLE OF INFORMATION COLLECTION: Preclinical Test Tracking and Management System (PTTMS) Survey


PURPOSE:

This survey will be used to collect feedback and user satisfaction for the Preclinical Test Tracking and Management System (PTTMS). The PTTMS will capture requests from external researchers to access DMID’s Preclinical Services Program and will include submission and execution of Non-Clinical Evaluation Agreements (NCEAs) and Service Request Forms (SRFs), as well as capturing test results from DMID contractors.


DESCRIPTION OF RESPONDENTS:


Respondents will include external requestors (outside of NIH) who access DMID’s Preclinical Services Program and DMID-funded contractors and DMID staff who administer the program.


TYPE OF COLLECTION: (Check one)


[ ] Customer Comment Card/Complaint Form [ ] Customer Satisfaction Survey

[X] Usability Testing (e.g., Website or Software [ ] Small Discussion Group

[ ] Focus Group [ ] Other: ______________________


CERTIFICATION:


I certify the following to be true:

  1. The collection is voluntary.

  2. The collection is low-burden for respondents and low-cost for the Federal Government.

  3. The collection is non-controversial and does not raise issues of concern to other federal agencies.

  4. The results are not intended to be disseminated to the public.

  5. Information gathered will not be used for the purpose of substantially informing influential policy decisions.

  6. The collection is targeted to the solicitation of opinions from respondents who have experience with the program or may have experience with the program in the future.


Name: Tracy N. LaPorte


To assist review, please provide answers to the following question:


Personally Identifiable Information:

  1. Is personally identifiable information (PII) collected? [] Yes [X] No

  2. If Yes, is the information that will be collected included in records that are subject to the Privacy Act of 1974? [] Yes [ ] No

  3. If Applicable, has a System or Records Notice been published? [ ] Yes [ ] No




Gifts or Payments:

Is an incentive (e.g., money or reimbursement of expenses, token of appreciation) provided to participants? [ ] Yes [X] No



ESTIMATED BURDEN HOURS and COSTS


Category of Respondent

No. of Respondents

No. of Responses per Respondent

Time per

Response

(in hours)

Total Burden

Hours

Private Sector

42

1

15/60

11

Totals


42


11



Category of Respondent


Total Burden

Hours

Hourly Wage Rate*

Total Burden Cost

Private Sector

11

$24.98

$274.78

Totals



$274.78

*https://www.bls.gov/oes/current/oes_nat.htm



FEDERAL COST: The estimated annual cost to the Federal government is $2048.10.


Staff


Grade/Step

Salary*

% of Effort

Fringe (if applicable)

Total Cost to Gov’t

Federal Oversight






Health Specialist

13/8

$122,310

1%


$1,223.10













Contractor Cost






Scientific Program Manager


$82,534

1%


$825

Travel






Other Cost












Total





$2048.10

*the Salary in table above is cited from https://www.opm.gov/policy-data-oversight/pay-leave/salaries-wages/salary-tables/pdf/2018/DCB.pdf








If you are conducting a focus group, survey, or plan to employ statistical methods, please provide answers to the following questions:


The selection of your targeted respondents

  1. Do you have a customer list or something similar that defines the universe of potential respondents and do you have a sampling plan for selecting from this universe? [ ] Yes [X] No


If the answer is yes, please provide a description of both below (or attach the sampling plan)? If the answer is no, please provide a description of how you plan to identify your potential group of respondents and how you will select them?


Respondents will be identified when they contact DMID staff to access the Preclinical Services Program.


Administration of the Instrument

  1. How will you collect the information? (Check all that apply)

[X] Web-based or other forms of Social Media

[ ] Telephone

[ ] In-person

[ ] Mail

[ ] Other, Explain

  1. Will interviewers or facilitators be used? [ ] Yes [ X ] No

Please make sure that all instruments, instructions, and scripts are submitted with the request.




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File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
File TitleGeneric Clearance Submission Template
SubjectGeneric Clearance Submission Template
AuthorOD/USER
File Modified0000-00-00
File Created2021-01-14

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