№ files_lp_3_process_9_35543
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Administrative standards outlining residency, income, insurance, and clinical eligibility requirements for enrollment in Maryland cancer screening, diagnostic, and treatment programs for fiscal year 2024.
Program Name/Jurisdiction:
Maryland Breast and Cervical Cancer Program and/or CRF Cancer Prevention, Education, Screening and Treatment Program
Fiscal Year:
2024
Document Type:
Administrative standards and eligibility guidelines
Geographic Scope:
Maryland, United States
Administering Authority:
Local Maryland cancer screening programs
Subject:
Eligibility criteria for screening, diagnostic, referral, and treatment services
Target Population:
Maryland residents seeking cancer screening and related services
Eligibility Criteria:
Residency, annual gross household income up to 250% of Federal Poverty Level, family size, insurance status
Verification Requirements:
Verbal or written proof of residency, income documentation, insurance verification, Medicaid status confirmation via EVS
Programs Referenced:
BCCP-CPEST Programs, Patient Navigation Only (PNO), Cancer Screening and Tracking (CaST), Client Database (CDB)
Standards Referenced:
Minimal Clinical Elements (MCE), Minimal Standards for Nursing Case Management
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2020
Region / City:
Clark County, Ohio
Topic:
Housing and Emergency Assistance Grants
Document Type:
Government Assistance Program
Organization:
Clark County Community & Economic Development
Author:
Dirk Lackovich-Van Gorp, Grants Coordinator
Target Audience:
Individuals, families, and households in Clark County, Ohio affected by COVID-19
Period of Validity:
March 1, 2020 – December 31, 2020
Approval Date:
October 14, 2020
Revision Date:
November 19, 2020
Year:
2025
Event:
October CRF Forum
Location:
Ft. Lauderdale, FL, USA
Type:
Conference agenda and ROI justification
Organizer:
Credit Research Foundation
Audience:
Company executives and finance professionals
Duration:
3 days
Purpose:
Present ROI and justify attendance costs
Key Topics:
Credit risk management, process innovation, cash flow optimization, benchmarking, professional development
Attachments:
Estimated investment breakdown, post-conference report plan
Year:
2019
Region / city:
Not specified
Subject:
Clinical trial documentation, Case Report Form (CRF) design
Document type:
SOP (Standard Operating Procedure)
Organization:
ALERRT (Association for Data Management in the Tropics)
Author:
Hanne Landuyt
Target audience:
Clinical trial staff, Data managers, Investigators
Period of validity:
Not specified
Approval date:
01/02/2019
Revision date:
10/10/2019
Date of changes:
20/06/2022
Year:
2015
Region / City:
Virginia
Topic:
Foster care, child safety, employee verification
Document Type:
Safety memorandum
Institution:
Virginia Department of Social Services, Department of Behavioral Health & Developmental Services
Author:
U.S. Department of Health & Human Services, Children’s Bureau
Target Audience:
Residential facilities for foster care children, facility administrators, human resource managers
Effective Period:
Ongoing
Approval Date:
September 1, 2014
Date of Changes:
September 21, 2015
Year:
2015
Region / City:
Not specified
Topic:
Clinical Trials, Data Management
Document Type:
SOP (Standard Operating Procedure)
Organization / Institution:
Clinical Research Center (CRC)
Author:
Not specified
Target Audience:
Research staff, investigators
Validity Period:
Not specified
Approval Date:
01/01/2015
Effective Date:
01/01/2015
Review / Revision Date:
01/01/2015
Year:
2023-2028
Region / city:
Norfolk, UK
Theme:
Equality, Diversity and Inclusion in Research
Document type:
Strategic Vision Statement
Organization / Institution:
NIHR Norfolk Clinical Research Facility
Author:
NIHR Norfolk CRF Management Team
Target audience:
Staff, patients, public research participants, healthcare professionals
Period of validity:
2023-2028
Approval date:
2023
Date of changes:
None
Year:
FY26
Region / City:
NHS Organisation
Subject:
NHS Organisation – FastTrack FRP
Document Type:
Claim Registration Form
Author:
Microsoft
Target Audience:
Eligible Microsoft FastTrack Ready Partners and NHS Organisations
Period of Action:
FY26
Date of Approval:
Not specified
Date of Changes:
Not specified
Year:
Not specified
Region / City:
Not specified
Topic:
Myasthenia Gravis monitoring
Document Type:
Case Report Form
Organization / Institution:
Clinical research study
Target Audience:
Clinical investigators, study coordinators
Assessment Tools:
MGFA Post Intervention Status, MG Scale, QMG Score, MG-MMT Score, MG-ADL Score, MG-QOL15 Score
Data Classification:
Core and supplemental elements
Frequency of Completion:
Every study visit
Patient Status Categories:
CSR, PR, MM-0, MM-1, MM-2, MM-3, Improved, Unchanged, Worse, Exacerbation, Died of MG
Instructions:
Includes general and specific guidance for CRF completion
Source Type:
Clinical research form
Structured Data:
Quantitative and qualitative assessment of MG severity and progression
Data Dictionary Reference:
Definitions and classifications of CRF elements included
Year:
2023
Region / city:
Belgium
Topic:
Legal and technical elements of an invoice
Document type:
Invoice
Organization:
Belgian VAT regulation authority
Author:
N/A
Target audience:
Companies and service providers in Belgium
Period of validity:
N/A
Approval date:
N/A
Amendment date:
N/A
Year:
2022
Month:
August
Document type:
Guidance and standardized study document
Subject:
Biological resources and environmental analysis
Issuing body:
California Department of Transportation
Division:
Division of Environmental Analysis, Office of Biological Studies
Jurisdiction:
State of California
Applicable programs:
State Highway System projects
Related standards:
Standard Environmental Reference (SER)
Compliance references:
Americans with Disabilities Act
Advisory group:
Biological Consultancy Group
Intended projects:
Minor A and B transportation projects with limited natural resource impacts
Preparation requirements:
Associate Environmental Planner (Natural Science) or equivalent
Source type:
Government technical guidance document
Year:
2023
Region / City:
Australia
Topic:
Mental Health Treatment Plan
Document Type:
Medical Form
Institution:
Medicare Australia
Author:
Unknown
Target Audience:
Healthcare Providers, General Practitioners
Validity Period:
From date of creation until the next review
Approval Date:
Not specified
Modification Date:
Not specified
Contextual Description:
A medical form detailing the minimal requirements for a GP mental health treatment plan, including patient information, assessment, interventions, and consent for sharing health data.
Note:
Year
Year:
2026
Region / City:
Palo Alto, Stanford
Topic:
Research Consent Template
Document Type:
Consent Form
Organization:
VA Palo Alto, Stanford University
Author:
VA Palo Alto Research Team
Target Audience:
Research Participants
Duration of Study:
Varies
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Subject:
Research Ethics
Document Type:
Template
Organization:
Medical College of Wisconsin
Target Audience:
Research participants
Institution:
University of British Columbia
Document type:
Clinical informed consent form template
Study risk level:
Minimal risk
Regulatory scope:
Not regulated by Health Canada or the U.S. Food and Drug Administration
Jurisdiction:
British Columbia, Canada
Intended use:
Non-regulated clinical research studies
Target audience:
Research participants from the general population
Reading level:
Grade 7
Applicable populations:
Adults and, where applicable, pediatric participants with parental permission and child assent
Ethics oversight:
Research Ethics Board (REB)
Source type:
Institutional research ethics documentation
Note:
Year
Topic:
Research Ethics
Document Type:
Consent Notice
Organization / Institution:
San Jose State University
Author:
Lisa Simpson, San Jose State University graduate student
Target Audience:
Participants in minimal risk research involving adults
Contextual Description:
A consent notice for a minimal risk research study involving adults, explaining participant rights, study procedures, and confidentiality measures.
Document type:
Informed consent form template
Research category:
Human subjects research
Risk level:
Minimal risk
Governing standards:
Institutional Review Board requirements; Associated Press Style Manual
Regulatory references:
U.S. Food and Drug Administration
Responsible organization:
Jaeb Center for Health Research IRB
Intended institutions:
Academic medical centers and affiliated health systems
Target audience:
Research participants and legally authorized representatives
Geographic context:
United States
Source type:
Institutional research ethics documentation
Note:
Authors
Website:
http://www.aamt.info/english/utx/
Status:
official release
Last updated:
March 19, 2019
Document language:
English
License:
CC0 1.0
Disclaimer:
See http://aamt.info/english/utx/index.htm#disclaimer
File structure:
tab-delimited text
File extension:
".utx"
Character encoding:
UTF-8 with BOM.
New line code:
"
" (CR+LF).
Line comment symbol:
# (hash symbol).
UTX version:
1.20
User-defined fields:
x-termUsage:en