№ files_lp_3_process_9_47918
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This document is a formal application for the joint providership of CME activities, detailing required disclosures and guidelines for financial relationships with ineligible companies, in compliance with ACCME standards.
Note:
Year
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Year:
2024
Note:
Region/City
Topic:
Continuing Medical Education
Document Type:
Application Form
Organization:
PALTmed
Target Audience:
Medical Directors, Social Workers, Physicians, Administrators, Nurses/Nurse Practitioners, Physician Assistants, Pharmacists
Year:
2026
Region:
United States
Document Type:
Fee Schedule
Organization:
PALTmed
Target Audience:
CME applicants, program organizers
Base Fee:
$750 (State Chapter), $1,500–$2,000 (Non-Chapter)
Per Credit Fee:
$40–$200 per CME credit hour
Additional Fees:
Incomplete Application Fee $300, Application Late Fee $300, Post-Conference Late Fee $300, Re-Review Fee $300
Applicable Credits:
CME, CMD, ABIM MOC
Conditions:
Fees vary by membership status, application completeness, and submission timing
Year:
2012/17
Region / City:
United States
Subject:
Postsecondary Education, Longitudinal Studies
Document Type:
Statistical Study
Agency / Institution:
National Center for Education Statistics, U.S. Department of Education
Author:
National Center for Education Statistics
Target Audience:
Researchers, Policymakers, Educational Institutions
Period of Action:
2017
Approval Date:
August 2016
Amendment Date:
April 2017
A document detailing the data collection procedures and methodology for the 2012/17 Beginning Postsecondary Students Longitudinal Study (BPS:
12/17) conducted by the U.S. Department of Education, including data collection instruments, testing, and confidentiality procedures.
Note:
Year
Document type:
Checklist
Organization / Institution:
ACT Teacher Quality Institute
Target audience:
Experienced teachers applying for full registration
Year:
2019
Country:
United States
Agency:
U.S. Department of Veterans Affairs
Office:
Office of Procurement, Acquisition and Logistics, Strategic Acquisition Center
Document type:
Justification and Approval Notice
Subject:
Extension of services for hospital beds for home use and assemblies
Contract number:
VA797N-14-C-0015
Modification number:
P00016
Awardee:
Invacare Corporation, Home Care Division
Period of performance:
November 23, 2019 to January 22, 2020
Estimated value:
Approximately $2.4 million
Statutory authority:
41 U.S.C. § 3304(a)(1); FAR 6.302-1; 38 U.S.C. § 8123
Contract type:
Firm-Fixed-Price
Procurement method:
Other than full and open competition
NAICS code:
339113
Location:
Fredericksburg, Virginia
Contextual description:
Federal procurement justification documenting the approval to extend an existing sole-source contract for the supply and servicing of hospital beds and related accessories for eligible veterans’ home use during a defined interim period.
Note:
Year
Subject:
Road Construction, Stabilization
Document Type:
Technical Specification
Organization / Institution:
Michigan Department of Transportation
Target Audience:
Contractors, Engineers
Year:
2024
Region / City:
N/A
Topic:
Program Accreditation
Document Type:
Checklist
Institution / Organization:
N/A
Author:
N/A
Target Audience:
Accreditation reviewers, program staff
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2026
Region / city:
N/A
Subject:
Client Protection Standards Audit
Document type:
Audit Report
Organization:
Cerise+SPTF
Author:
N/A
Target audience:
FSP Management, Investors, Microfinance Experts, Stakeholders
Period of validity:
N/A
Approval date:
18 January 2026
Date of revisions:
N/A
Year:
2025
Jurisdiction:
Texas, United States
Subject:
Criminal justice information systems operations and access
Document type:
Operational manual
Issuing body:
Texas Department of Public Safety
Systems covered:
Texas Crime Information Center; Texas Law Enforcement Telecommunications System; National Crime Information Center; Nlets
Bureau:
Compliance and Training Bureau
Access level:
Sensitive but unclassified
Intended audience:
Law enforcement agencies and criminal justice administrators
Effective date:
January 1, 2025
Contact information:
[email protected]
RECOGNITION OF DISTINCTION 2026 CONFERMENT OF THE TITLE OF FULL PROFESSOR INFORMATION FOR APPLICANTS
Year:
2026
Region / City:
Oxford
Subject:
Academic titles
Document Type:
Application Guide
Organization / Institution:
University of Oxford
Author:
University of Oxford
Target Audience:
Applicants for the position of Full Professor
Period of Validity:
From November 17, 2025, to January 15, 2026
Approval Date:
N/A
Date of Changes:
N/A
Year:
2026
Event:
7th fib Congress
Location:
Lisbon, Portugal
Document Type:
Template / Instructions
Target Audience:
Authors submitting full papers to the Congress
Language:
English
Format:
PDF, A4, Times New Roman
Page Range:
8–10 pages
Submission Platform:
https://fiblisbon2026.pt
Note:
/ www.conftool.pro/fiblisbon2026
Keywords:
keyword1, keyword2, keyword3, keyword4, keyword5
Corresponding Author:
indicated with * and email provided
Year:
2026
Region / City:
Selangor, Malaysia
Subject:
Academic Paper Formatting
Document Type:
Template
Organization / Institution:
Universiti Kebangsaan Malaysia, Pusat PERMATA@Pintar Negara
Author:
Noreen Ayob, Chong Fei Sze, Mohd Anuar Arsyad
Target Audience:
Researchers, Academics, Conference Participants
Period of Validity:
Not Specified
Approval Date:
Not Specified
Date of Changes:
Not Specified
Year:
2026
Region / City:
Not specified
Topic:
Academic Paper Submission Guidelines
Document Type:
Paper Submission Template
Institution / Organization:
Not specified
Author:
Not specified
Target Audience:
Researchers and Authors submitting academic papers
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Context
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:
Grossmont Healthcare District
Topic:
Grant Application
Document Type:
Full Grant Application
Organization / Institution:
Grossmont Healthcare District
Author:
Grossmont Healthcare District
Target Audience:
Nonprofit organizations, grant applicants
Period of Validity:
FY 25-26
Approval Date:
Not provided
Date of Changes:
Not provided
Year:
Not specified
Region / City:
Not specified
Subject:
Health check, intellectual and developmental disabilities, medical management
Document Type:
Health checklist
Institution:
Not specified
Author:
Not specified
Target Audience:
Healthcare professionals working with adults with intellectual and developmental disabilities
Effective Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Year:
2024
Region / City:
European Union
Theme:
Health Technology Assessment
Document Type:
Guidance Document
Author:
HTA Coordination Group (HTACG)
Target Audience:
Health Technology Developers, Regulatory Authorities, Medical Researchers
Period of Validity:
Ongoing
Approval Date:
28 November 2024
Date of Last Change:
N/A
Context:
Guidance document for filling in the joint clinical assessment (JCA) dossier template for medicinal products, intended for use by health technology developers and regulatory bodies.
Year:
2021
Region / City:
Africa
Topic:
Youth empowerment, social development, regional cooperation
Document type:
Workplan and results framework
Organ / Institution:
UNDP, YCA Hub
Author:
UNDP Regional Youth Team
Target audience:
Government agencies, youth organizations, development partners, UNDP Country Offices
Validity period:
2021
Approval date:
Not specified
Date of amendments:
Not specified
Year:
2019
Region / City:
European Union
Topic:
PRIIPs Regulation amendments
Document Type:
Consultation Paper
Institution:
European Supervisory Authorities (ESAs)
Author:
European Supervisory Authorities (ESAs)
Target Audience:
Stakeholders in financial services and investments
Action Period:
16 October 2019 - 13 January 2020
Approval Date:
16 October 2019
Amendment Date:
Not specified