Application for NIH Support to Participate in Industry and Investor Showcase Events

Sub-Study Template - Application for NIH Support to Participate in Industry and Investor Showcase Events (002).doc

Conference, Meeting, Workshop, and Poster Session Registration Generic Clearance (OD)

Application for NIH Support to Participate in Industry and Investor Showcase Events

OMB: 0925-0740

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Request for Approval under the “Conference, Meeting, Workshop, and Poster Session Registration Generic Clearance (OD)”

(OMB#: 0925-0740 Exp Date: 05/2019)

T ITLE OF INFORMATION COLLECTION: Application for NIH Support to Participate in Industry and Investor Showcase Events


PURPOSE:

The information collection encompassed by this form will allow the NIH to select the most appropriate participants for non-grantee activities sponsored, organized, and run by NIH staff, according to the type and purpose of the activity. For NIH to plan and conduct activities that are timely for participants in their field of research, it is often necessary for such information to be collected within a relatively short turnaround time. In general, submitted application materials will be reviewed by an internal NIH committee responsible for planning activities. However, application materials may be shared with conference organizers outside of NIH. The committee and/or conference organizers will be responsible for selecting and notifying participants. It is fully anticipated that the applicants will have the requested information readily available, minimizing the burden on each applicant. It is expected that this form will be used to select participants for 10 conferences per year.



DESCRIPTION OF RESPONDENTS:

All respondents will be health professionals who represent small businesses that have received funding from the NIH through the SBIR/STTR programs. It is anticipated that each conference will receive 50 applications.




TYPE OF COLLECTION: (Check one)


[ ] Abstract [X] Application

[ ] Registration Form [ ] 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.


Name:__John Sheridan, Ph.D.__________________________________


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


Personally Identifiable Information:

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

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


Gifts or Payments:

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

Amount: ___________

Explanation for incentive: (include number of visits, etc.)




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 (for-profit)

500

1

1

500






Totals

500

500


500



Category of Respondent


Total Burden

Hours

Wage Rate*

Total Burden Cost

Health Professionals

500

$35.93

$17,965





Totals

500


$17,965


*Cite source per bls.gov if applicable: This estimate is based on the following data from the Bureau of Labor Statistics: The Health Professionals wage rate was obtained from http://www.bls.gov/oes/2013/may/oes290000.htm occupation title “Healthcare Practitioners and Technical Occupations”, occupation code 29-0000.



FEDERAL COST: The estimated annual cost to the Federal government is $1,965.78


Staff


Grade/Step

Salary

% of Effort

Fringe (if applicable)

Total Cost to Gov’t

Federal Oversight






Program Analyst

GS-13, Step 3

$98,289

2%


$1,965.78













Contractor Cost












Travel





$1,965.78

Other Cost




















The selection of 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? [X] Yes [ ] 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?


Active and/or recently awarded NIH SBIR/STTR awardees will be eligible to apply to participate in NIH-supported industry and investor showcase events. Certain events focus on a specific technology field (e.g., medical devices), thus a subset/sampling of awardees may be asked to complete the form.


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

[X] Mail

[ ] Survey form

[ ] Chart Abstraction

[ ] Other, Explain


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

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


Instructions for completing Request for Approval under the “United States and Global Human Influenza Surveillance in at-risk Settings”


PLEASE DO NOT SUBMIT INSTRUCTIONS WITH FINALREQUEST



TITLE OF INFORMATION COLLECTION: Provide the name of the collection that is the subject of the request. (e.g. Comment card for soliciting feedback on xxxx)


PURPOSE: Provide a brief description of the purpose of this collection and how it will be used. If this is part of a larger study or effort, please include this in your explanation.


DESCRIPTION OF RESPONDENTS: Provide a brief description of the targeted group or groups for this collection of information. These groups must have experience with the program.


TYPE OF COLLECTION: Check one box. If you are requesting approval of other instruments under the generic, you must complete a form for each instrument.


CERTIFICATION: Please read the certification carefully. If you incorrectly certify, the collection will be returned as improperly submitted or it will be disapproved.


Personally Identifiable Information: Provide answers to the questions.


Gifts or Payments: If you answer yes to the question, please describe the incentive and provide a justification for the amount.


BURDEN HOURS and COSTS:

Category of Respondents: Identify who you expect the respondents to be in terms of the following categories: (1) Individuals or Households; (2) Private Sector ( for profit or not-for-profit); (3) State, local, or tribal governments; or (4) Federal Government. Only one type of respondent can be selected per row.

No. of Respondents: Provide an estimate of the number of respondents.

Average Burden per Response: Provide an estimate of the amount of time required for a respondent to participate (e.g. fill out a survey or participate in a focus group). Describe the amount in fractions if the time is less than an hour (e.g., 5 minutes would be 5/60)

Total Burden Hours: Provide the number of burden hours by multiplying the # of responses x the # of responses per respondent x the average burden per response.

Burden Cost: Multiply Total Burden Hours x Wage Rate to get the Total Burden Cost.


FEDERAL COST: Provide an estimate of the annual cost to the Federal government. Fill out table to itemize the Federal cost of the collection. At a minimum there should be Federal cost.


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. Please provide a description of how you plan to identify your potential group of respondents and how you will select them. If the answer is yes, to the first question, you may provide the sampling plan in an attachment.


Administration of the Instrument: Identify how the information will be collected. More than one box may be checked. Indicate whether there will be interviewers (e.g. for surveys) or facilitators (e.g., for focus groups) used.


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


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File Typeapplication/msword
File TitleGeneric Clearance Submission Template
SubjectGeneric Clearance Submission Template
AuthorOD/USER
Last Modified ByFountain, Marisa (NIH/OD) [E]
File Modified2016-07-19
File Created2016-07-19

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