№ files_lp_3_process_7_034580
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Summary of a public health meeting agenda and notes detailing proposed revisions to Zika virus case definitions, clinical criteria for congenital and pregnancy-related complications, and reporting procedures to CDC pregnancy registries.
Year:
2016
Region / City:
United States, national
Topic:
Zika virus surveillance and case definitions
Document Type:
Meeting agenda / conference call notes
Organization / Institution:
Council of State and Territorial Epidemiologists (CSTE), CDC
Speakers / Contributors:
Joe McLaughlin, Marc Fischer, Peggy Honein, Frederic E. Shaw
Target Audience:
State epidemiologists, public health officials
Period Covered:
May 23, 2016
Date of Publication:
May 23, 2016
Proposed Changes:
Revisions to Zika virus interim case definitions, expansion of clinical criteria, pregnancy registry reporting
Surveillance Details:
Non-congenital and congenital Zika virus infection case classifications, laboratory testing protocols
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Year:
TBD
Region / City:
Florida, Indiana, Kansas, Maryland, Michigan, Minnesota, New Hampshire, New Jersey, New York, North Carolina, Ohio, Oregon, Tennessee, Texas, Virginia
Topic:
Electronic Health Record Access for State Health Departments
Document Type:
Email
Organization:
Centers for Disease Control and Prevention (CDC), Association of State and Territorial Health Officials (ASTHO)
Author:
Project Contractor
Target Audience:
Health Department HAI Coordinators, Epidemiologists
Effective Period:
TBD
Approval Date:
TBD
Modification Date:
TBD
Year:
2025
Region / City:
Boulder City
Theme:
Community Engagement
Document Type:
Speech Transcript
Organization:
Boulder City Council
Author:
Mayor Michele Romero
Target Audience:
Community members, local leaders, and city staff
Period of Action:
2025
Approval Date:
2025
Date of Changes:
N/A
Year:
2026
Region / City:
United States
Topic:
Federal procurement and contract management
Document Type:
Policy/Guidance
Agency / Institution:
GSA (General Services Administration)
Author:
GSA
Target Audience:
Contractors, Government Agencies
Period of Validity:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Year:
2024
Region / City:
United Kingdom
Subject:
Tender for data services
Document Type:
Invitation to Tender
Organ / Institution:
UK Sport
Author:
UK Sport
Target Audience:
Potential Tenderers for Data Services
Period of Action:
April 2025 - March 2029
Approval Date:
19th November 2024
Date of Changes:
N/A
Year:
2023
Region / City:
Foothills
Topic:
HOA Dues, Operating Costs, Board Decisions
Document Type:
Notice
Organization / Institution:
Foothills HOA Board
Author:
Foothills HOA Board
Target Audience:
Homeowners
Effective Period:
From March 2023 onwards
Approval Date:
March 30, 2023
Amendment Date:
None
Year:
2026
Organization:
Preschool Access for All Learning Network
Document Type:
Mini-Grant Guidance
Target Audience:
Educators, Paraprofessionals, District Inclusion Teams
Age Group:
Children with disabilities, ages 3–5
Focus Areas:
Inclusive opportunities, developmentally appropriate environments, high-quality instruction
Expenditure Categories:
Instructional supplies and materials, in-service/staff development
Contact:
Misty Moody, Assistant Commissioner of Early Learning, [email protected]
Document Purpose:
Provide guidelines for mini-grant expenditures to support inclusion and developmentally appropriate practices
Year:
2025
Region / City:
Cincinnati, OH
Subject:
Documentary
Document Type:
Film
Organization:
PBS
Author:
Yemi Oyediran
Target Audience:
General Public
Effective Date:
October 10, 2025
Date of Approval:
September 18, 2025
Description:
A documentary film about the history and cultural impact of King Records, shedding light on its groundbreaking role in American music.
Year:
2020
Region / City:
USA
Topic:
Biosafety, Laboratory Systems, Public Health
Document Type:
Email Communication
Organization / Institution:
Centers for Disease Control and Prevention (CDC)
Author:
Division of Laboratory Systems, CDC
Target Audience:
Laboratory professionals, clinicians, and leadership in rural and community hospitals
Period of Action:
Not specified
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2026
Region / City:
N/A
Topic:
Consultant Contract DBE Information
Document Type:
Form
Institution / Organization:
Caltrans
Author:
N/A
Target Audience:
Consultants, Local Agencies, Caltrans
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
20XX
Region / city:
Texas
Subject:
Thesis/Dissertation
Document Type:
Thesis/Dissertation Template
Author:
[Insert full name here]
Target Audience:
Graduate Students, Academic Institutions
Period of Action:
[Month and year of graduation]
Date of Approval:
[Month and year]
Date of Changes:
[If applicable]
Year:
[year]
Degree:
[Degree Name]
Institution:
The University of Texas at El Paso
Department:
Graduate School
Author:
[Student’s Full Official Name]
Advisor:
[Committee Member Names]
Program:
[Program Name]
Acknowledgments:
Yes
Abstract:
Yes
References:
Yes
Glossary:
Yes
Appendix:
Yes
Vita:
Yes
Type:
Thesis or Dissertation
Date of Submission:
[Month, Year]
Year:
2025
Region / City:
New York, USA
Subject:
Immigration, Habeas Corpus
Document Type:
Legal Memorandum
Organization / Institution:
United States District Court for the Southern District of New York
Author:
[Client Name]
Target Audience:
Legal professionals, Court
Period of Validity:
Ongoing
Approval Date:
[Date]
Date of Changes:
[Date]
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:
2023
Region / City:
New York State
Theme:
Cultural Resource Management
Document Type:
Template for Historic Preservation Finding Document
Agency / Institution:
New York State Department of Transportation (NYSDOT)
Author:
Not specified
Target Audience:
Project managers, cultural resource coordinators, historical preservation professionals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2021
Region / city:
Various locations
Theme:
Publications and Dissemination Activities
Document type:
Report
Organization / institution:
ITEA 3
Authors:
ARD Group, BEIA Gmbh, Caretronic d.o.o., Dogus Technology, Experteam, FrontEndART Software, FTP - LDA, Hiperlink, ISEP, Strategy Big data, University of Szeged
Target audience:
Researchers, healthcare professionals, technology innovators
Period of validity:
2021-2024
Approval date:
01.01.2022
Date of modifications:
None
Year:
2022
Region / City:
Europe
Theme:
Space, Innovation, Research and Development
Document Type:
Call for Expression of Interest
Organization / Institution:
European Commission Directorate-General for Defence Industry and Space
Author:
European Commission
Target Audience:
Research entities, space technology developers, universities, and companies in the space sector
Period of Validity:
31 May 2022
Approval Date:
31 May 2022
Date of Last Change:
N/A
Year:
2021
Organization:
European Commission
Service:
Service for Foreign Policy Instruments (FPI)
Programme:
European Peace Facility (EPF)
Type of document:
Call for expression of interest
Place of employment:
Brussels
Unit:
FPI.5
Job profiles:
Audit assistance; Legal advice including anti-fraud, data protection and access to documents
Grades:
FG III; FG IV
Number of posts:
2
Eligibility:
Contract agents in EU institutions; EPSO CAST reserve list or database candidates
Languages required:
English; French
Application deadline:
23/08/2021
Recruitment period:
From October 2021
Contract type:
Contract agent under Article 3b CEOS
Security requirement:
Security clearance up to SECRET UE/EU SECRET or willingness to undergo vetting
Contact:
[email protected]
Year:
2019
Region / city:
Afghanistan
Theme:
Proposal for NAP 1325 Workshops
Document Type:
Call for Proposal
Organization:
UN Women
Author:
UN Women Afghanistan Country Office
Target Audience:
National NGOs, Civil Society Organizations, and Companies
Validity Period:
From 10th February 2019
Approval Date:
10th January 2019
Amendment Date:
N/A