№ lp_2_1_17769
File format: docx
Character count: 2858
File size: 24 KB
Note:
Year
Description:
List of patients and their associated challenges in different medical categories.
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Year:
2017
Region / City:
United States
Subject:
Software Documentation
Document Type:
User Manual
Organization:
Department of Veterans Affairs (VA)
Author:
REDACTED
Target Audience:
VA Medical Personnel
Validity Period:
Not specified
Approval Date:
June 2017
Date of Changes:
Ongoing revisions
Year:
2022
Region / City:
Des Moines, IA
Subject:
Medicaid Services, Procurement Process
Document Type:
Request for Proposal (RFP)
Organization:
Iowa Department of Human Services (DHS)
Author:
Kristin Jones
Target Audience:
Bidders, Contractors, Medicaid Service Providers
Period of Validity:
Not specified
Approval Date:
February 21, 2022
Amendment Date:
February 21, 2022
Year:
2010
Region / city:
United States
Topic:
Mobile Electronic Documentation Software Installation
Document Type:
Installation Guide
Organization / Institution:
Department of Veterans Affairs (VA)
Author:
MED Development Team
Target Audience:
IT personnel, system administrators
Period of validity:
Not specified
Approval date:
June 2010
Revision date:
September 2011
Year:
2026
Region / City:
United States
Theme:
Refugee support, microenterprise development
Document Type:
Instructional Form
Organization / Institution:
Office of Refugee Resettlement (ORR)
Author:
Not specified
Target Audience:
Recipient organizations and other MED program stakeholders
Period of Validity:
Ongoing throughout the 5-year project period
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2017
Month:
June
Document type:
Technical manual
Product name:
Mobile Electronic Documentation (MED)
Software version:
Client Software Version 2.3.311.6
Documentation patch:
TIU1.0311
Server patch:
TIU1.0257
Organization:
Department of Veterans Affairs
Office:
Office of Information & Technology
Division:
Product Development
Revision history period:
2011–2017
Subject area:
Health information technology
Intended system:
VA VistA and CPRS environment
Language:
English
Department:
Department of Veterans Affairs
Office:
Office of Information and Technology (OIT)
Document type:
Technical manual
System:
Mobile Electronic Documentation (MED)
Related system:
CPRS, VistA
Software component:
TIU MED GUI
Revision:
2.9
Revision date:
December 2025
Patch reference:
TIU1.0374
Authoring body:
CPRS Development Team
Audience:
Technical staff and system administrators
Compliance standard:
Section 508
Revision history period:
2011–2025
Note:
Revision History
Year:
2025
Region / City:
United States
Subject:
Mobile Electronic Documentation for VA Medical Records
Document Type:
User Manual
Organization:
Department of Veterans Affairs, Office of Information and Technology
Author:
CPRS Development Team
Target Audience:
VA medical staff and administrators
Period of validity:
December 2025
Approval Date:
December 2025
Date of last revision:
12/2025
Document title:
MED – List of Equipment to be Approved
Regulatory framework:
Directive (EU) 2025/1533
Subject area:
Marine equipment; Life-Saving Appliances
Related conventions and codes:
SOLAS; MARPOL; LSA Code; HSC Code 1994 + 2000
Referenced standards:
EN 60945:2002; IEC 60945 Corr.1:2008; ISO 24408:2005; ISO 15736:2006; ISO 15372:2000 incl. A1:2021
Certification modules:
B + D; B + E; B + F; G
Conformity assessment:
EC-Type-Examination Certificate
Involved bodies:
Notified Bodies
Content structure:
Item numbers MED/1.1 to MED/1.27
Equipment categories:
Lifebuoys; Life jackets; Liferafts; Lifeboats; Rescue boats; Launching appliances; Pyrotechnics; Marine evacuation systems
Year:
2020–2021; 2024–Present
Region / city:
Boston, MA; Waltham, MA; Woonsocket, RI; Springfield, MA; Marlborough, MA; Billerica, MA; San Diego, CA
Industry:
Biotech, Medical Devices, Healthcare
Document Type:
Resume/Curriculum Vitae
Organization / Institution:
ClearRock, Orbia, CVS Health, Baystate Health, Roche Diagnostics, Philips Healthcare, Biogen, Analog Devices, Affymetrix
Author:
Ken Halpin
Target Audience:
HR professionals, executives, and hiring managers in biotech, medical device, and healthcare sectors
Date of Approval:
Not specified
Date of Modifications:
Not specified
Year:
2022
Region / City:
Des Moines, Iowa
Subject:
Provider Cost Audits and Rate Setting Services
Document Type:
Notice of Intent to Award
Issuing Agency:
Department of Health and Human Services
Author:
Lisa Burk
Target Audience:
Bidders
Effective Period:
From November 10, 2022
Approval Date:
November 10, 2022
Modification Date:
N/A
Year:
2016/17
Region / city:
Wandsworth
Topic:
Healthcare Services, Clinical IT, Medical Guidelines
Document Type:
Guidelines
Target Audience:
Healthcare professionals, medical staff
Effective Period:
2016-2017
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2023
Region / City:
Not specified
Subject:
Child welfare, neglect investigation
Document Type:
Referral form
Agency:
CRC
Author:
Not specified
Target Audience:
Investigators, child welfare professionals
Period of Effectiveness:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2022-2023
Program:
EDEA MEd
Course:
Various courses in K12 & HE
Assessment Type:
Scoring of Assessments Related to Grades
Target:
A+, A, A-
Acceptable:
B+, B, B-, C+, C
Unacceptable:
C-, D+, D, D-, F
Evidence:
No evidence = assignment not submitted
Date of Evaluation:
November 7, 2024
Standards:
EDEA MEd Standards and Program Learning Objectives
Institutional Learning Objectives:
ILO 1, ILO 2, ILO 3, ILO 4, ILO 5, ILO 6, ILO 7
Scope:
Courses include subjects such as Final Research Project, Case Study, Final Capstone Project, and Peer Review of Projects
Assessment Coverage:
K12 and Higher Education
Audience:
Educational leaders, instructors, students in educational programs
Description:
Document outlines the assessment scores for various courses within the EDEA MEd program, detailing grade targets, acceptable scores, and the related standards and institutional learning objectives for the academic year.
Year:
2020
Programme:
ENI CBC Med
Project:
MED GAIMS
Duration:
September 2019 – August 2022
Countries involved:
Lebanon, Jordan, Spain, Italy
Document type:
Guidelines for sub-grant applications
Responsible organization:
MED GAIMS Consortium
Funding:
European Union
Target audience:
Game developers, tourism entrepreneurs
Total funding allocated:
EUR 240,000
Maximum grant per digital game:
EUR 15,000
Maximum grant per analog game:
EUR 10,000
Equipment allowance:
Up to EUR 5,000 per project
Number of sub-grants:
20 (5 per country)
Application requirements:
Eligibility criteria, simplified cost calculation, output-based deliverables
Note:
Year
Subject:
Blood Borne Virus Testing, HIV, Hepatitis B, Hepatitis C
Document Type:
Procedure
Organization / Institution:
Canberra Health Services
Target Audience:
Medical Officers, nurses, midwives, students under supervision
Version:
1.5.0.0
Protocol Posting Date:
June 2024
CAP Laboratory Accreditation Program Protocol Required Use Date:
March 2025
Authors:
Gulisa Turashvili, MD, PhD; Uma G. Krishnamurti, MD, PhD; Barbara A. Crothers, DO; Giovanna A. Giannico, MD; Krisztina Hanley, MD; Anna Plotkin, MD; Anthony N. Karnezis, MD, PhD.
Note:
Accreditation Requirements
Date of Protocol Posting:
June 2024
Date of Required Use:
March 2025
Year:
2021
Region / City:
United Kingdom
Subject:
Assistance Dogs, Emergency Ambulance Services
Document Type:
Procedure
Organization / Institution:
South East Coast Ambulance Service NHS Foundation Trust
Author:
Not specified
Target Audience:
Ambulance Service Staff
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Version:
NENC v2.0
Date published:
22 January 2026
Planned review date:
October 2027
Region:
North East and North Cumbria
Healthcare system:
NHS
Clinical area:
Neurology
Condition:
Amyotrophic lateral sclerosis
Medicine:
Riluzole
Document type:
Shared care protocol
Indication:
Extension of survival or time to mechanical ventilation in ALS
Target population:
Adults
Intended audience:
NHS healthcare professionals
Initiating authority:
Neurological specialist services
Regulatory reference:
NICE Technology Appraisal TA20
Prescribing setting:
Secondary to primary care transfer
Monitoring requirements:
Liver function tests, full blood count, urea and electrolytes
Route of administration:
Oral or enteral
Licensing status:
Licensed for ALS only
Year:
2024
Region / City:
Australia
Document Type:
Regulatory submission for PBS listing
Organization:
Biogen Australia Pty Ltd
Drug Name:
Omaveloxolone (Skyclarys®)
Indication:
Friedreich’s ataxia in adults and adolescents aged 16 years and older
Dosage Form:
Capsule 50 mg, oral administration
Regulatory Status:
Orphan drug status granted by TGA, EMA and FDA approvals
Submission Date:
26 June 2024
PBAC Meeting:
March 2025
Population:
Patients aged 16 years and older with Friedreich’s ataxia
Treatment Phase:
Initial and continuing treatment
Prescriber Type:
Dental, Medical Practitioners, Nurse Practitioners, Optometrists
Restriction Type:
Authority Required (telephone/online PBS Authorities system)
Clinical Criteria:
Genetic confirmation of FXN mutation, presence of clinical symptoms, management under a specialist or consultation with specialized unit if needed
Treatment Criteria:
Must be given with best supportive care, hemodynamically stable in case of cardiac history
Administrative Advice:
Queries directed to Services Australia, prescribing information available online