№ files_lp_4_process_3_084021
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Email invitation requesting feedback from participants of the 2024 EIS match process through a brief anonymous survey.
Year:
2024
Organization:
Centers for Disease Control and Prevention (CDC)
Document type:
Survey invitation email
Target audience:
Incoming 2024 EIS Officers, Recruiters, EIS Program Staff
Survey link:
https://www.surveymonkey.com/r/2024EISMatch
Expiration date:
06/30/2025
Send date:
May 9, 2024
Survey closing date:
May 23, 2024 at 11:59 pm ET
Contact email:
[email protected]
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2017
Region / city:
Eatontown, NJ
Subject:
Enterprise Infrastructure Solution (EIS) Management Software Request for Information (RFI)
Type of document:
Request for Information (RFI)
Organization / institution:
Department of Veterans Affairs, Technology Acquisition Center
Author:
Michael Frank
Target audience:
Contractors in telecommunications and related services
Period of validity:
August 30, 2017
Approval date:
August 30, 2017
Date of modifications:
None
Year:
2019
Region / City:
United States
Topic:
Market Research for Endoscopy Information Systems (EIS)
Document Type:
Sources Sought Notice
Organ / Institution:
Veterans Health Administration (VHA)
Author:
Charles W. Herring
Target Audience:
Potential vendors for Endoscopy Information Systems
Period of Validity:
N/A
Approval Date:
09-25-2019
Amendment Date:
N/A
Year:
2023
Region / City:
Queensland, Australia
Subject:
Environmental Impact Statement (EIS) Notification
Document Type:
Public Notice
Authority:
Department of Environment, Science and Innovation
Author:
Not specified
Target Audience:
Government agencies, affected persons, and the public
Period of Validity:
Submission period minimum 30 business days
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
1994
Region / city:
Queensland, Australia
Topic:
Environmental Impact Assessment (EIA), Environmental Protection Act
Document Type:
Guideline
Organization / Institution:
Department of Environment, Science and Innovation (DESI)
Author:
Department of Environment, Science and Innovation (DESI)
Target Audience:
Proponents, consultants, stakeholders in the environmental assessment process
Effective Period:
Ongoing
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
2010
Organization:
Centers for Disease Control and Prevention (CDC)
Program:
Epidemic Intelligence Service (EIS) Fellowship
Document Type:
Data Elements Reference
Audience:
EIS alumni and program administrators
Content Scope:
Login, registration, contact information, education, training, skills, professional experience, directory, emails, program differences, list of values
Sections:
Introduction, Login and Registration Pages, Electronic Consent, Contact Information, Education/Training/Skills, Professional Experience, Directory, Appendices A-C
Purpose:
To list and structure all data elements collected from EIS program alumni
Format:
Tables with column names, labels, entities, figures, and value lists, accompanied by screenshots
Language:
English
Year:
2022
Region:
Federal
Subject:
Environmental Impact Statement (EIS) Preparation
Document Type:
Procedural Guide
Author:
Federal Highway Administration (FHWA)
Target Audience:
Transportation Project Managers, Environmental Coordinators, Federal Agencies
Period of Validity:
Ongoing
Approval Date:
July 2022
Modification Date:
Not specified
Year:
2020
Region / City:
Online
Topic:
Change Request
Document Type:
Technical Specification
Author:
Rohde & Schwarz
Target Audience:
Technical experts and engineers
Period of validity:
Not specified
Approval Date:
2020-10-22
Change Category:
F (correction)
Release:
Rel-15
Work Item Code:
NR_newRAT-Core
Reason for Change:
The abbreviation for EIS is explained inconsistently in the specification.
Summary of Change:
Update definition of EIS in chapter 3.1.
Consequences if not approved:
Inconsistent definition remains in the specification.
Clauses Affected:
3.1
Other Specifications Affected:
TS/TR 38.521-2
Other Comments:
None
Note:
Year
Contextual Description:
A non-disclosure agreement regarding confidential information related to the GSA EIS Program.
Year:
2024
Region / City:
N/A
Topic:
EIS Recruitment and Match Process Feedback
Document Type:
Survey
Agency / Institution:
CDC
Author:
N/A
Target Audience:
EIS Officers, EIS Program Participants, Recruiters
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2022
Organization:
Centers for Disease Control and Prevention (CDC)
Department:
EIS Program
Document Type:
Email
Audience:
Incoming 2022 EIS Officers, Recruiters, Program Staff
Date Sent:
May 23, 2022 and May 31, 2022
Survey Link:
https://www.surveymonkey.com/r/2022EISMatch
Estimated Completion Time:
6 minutes
Purpose:
Collect feedback on the 2022 EIS Virtual Match process
Year:
2021
Region:
United States
Theme:
Public health workforce recruitment
Document Type:
Survey
Organization:
Centers for Disease Control and Prevention (CDC)
Author:
EIS Program
Target Audience:
Incoming and current EIS officers, recruiting supervisors
Data Collection Method:
Online survey
Expiration Date:
5/31/2022
Survey Topics:
Recruitment experience, coaching, interviews, use of Slack, overall match satisfaction
Response Format:
Likert scale and open-ended questions
Confidentiality:
Anonymous responses
Estimated Completion Time:
5 minutes
Contains:
Instructions for navigation and contact information
Year:
2023
Region / City:
United States
Theme:
EIS Program, Recruitment, Survey
Document Type:
Email Invitation
Organization / Institution:
CDC (Centers for Disease Control and Prevention)
Author:
EIS Program
Target Audience:
2023 EIS Officers, Recruiters, EIS Program Staff
Effective Date:
May 8, 2023
Date of Changes:
May 22, 2023
Year:
2026
Region / city:
Walcha, New England Tablelands, Australia
Topic:
Environmental and social impact assessment
Document type:
Objection letter / Community submission
Organization / institution:
Glen Collin Pastoral Co.
Author:
Fiona Thompson (nee Young)
Target audience:
Vestas, project developers, local community
Period covered:
Planning and construction phase of Winterbourne Wind Project
Date submitted:
2026
Key concerns:
Social impact, environmental impact, economic impact, community consultation, road infrastructure, biodiversity, water usage, tourism
Year:
Not provided
Region / City:
Not specified
Topic:
Research ethics, manuscript submission
Document type:
Template
Author:
Not specified
Target audience:
Authors submitting research articles
Period of validity:
Not provided
Approval date:
Not specified
Date of changes:
Not specified
Investigator:
[insert name of principal investigator]
Key Information:
The following is a short summary of this study to help you decide whether or not to be a part of this study. More detailed information is listed later on in this form.
Note:
Why am I being invited to take part in a research study?
You will be asked to _________ [include a high level summary of the procedures that will be done. For example:
You will be given an investigational drug and asked to come for 3 study visits. You will give a total of 3 blood samples and fill out questionnaires asking about how you feel.]
Instead of being in this research study, your choices may include:
[List alternatives procedures. For student subject pools describe alternatives for course credit. For clinical trials describe the options that you would normally offer patient. If applicable, include supportive care as an option.]
Detailed Information:
The following is more detailed information about this study in addition to the information listed above.
[Tell the subject what to expect using lay language and simple terms. Whenever appropriate include the following items:
]
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Year:
2025
Region / City:
Hills
Theme:
Bowls competition regulations
Document Type:
Rules
Organization:
Hills Bowling Association
Author:
Hills Bowling Association Executive Committee
Target Audience:
Affiliated Clubs, Players, Officials
Period of Validity:
Ongoing
Approval Date:
6.1.25
Date of Amendments:
6.1.25
Year:
2022
Region / City:
United States
Topic:
Education, Financial Flexibility
Document Type:
Official Letter
Organization / Institution:
United States Department of Education, Office of Postsecondary Education
Author:
Michelle Asha Cooper, Ph.D.
Target Audience:
GEAR UP Grantee Project Directors
Effective Period:
From March 13, 2020, to September 30, 2023
Approval Date:
July 27, 2022
Amendment Date:
None