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This document provides guidelines for completing the AMFE Tool, including the midpoint and endpoint evaluations, for undergraduate social work students.
Note: Year
Subject: Social Work
Document Type: Guide
Institution: University of Akron
Target Audience: Undergraduate Students in Social Work
Price: 8 / 10 USD
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MassHealth Delivery System Reform Incentive Payment Program Midpoint Assessment Community Partner Report: Behavioral Health Network, Inc. (December 2020)
Year: 2020
Program: MassHealth Delivery System Reform Incentive Payment Program
Report type: Independent midpoint assessment report
Organization assessed: Behavioral Health Network, Inc.
Independent assessor: The Public Consulting Group
Commissioning authority: MassHealth
Geographic scope: Massachusetts
Assessment period: July 1, 2017–December 31, 2019
Community Partner program implementation date: July 18, 2018
Focus areas: Organizational Structure and Engagement; Integration of Systems and Processes; Workforce Development; Health Information Technology and Exchange; Care Model
Methodology: Qualitative assessment based on document review and key informant interviews
Data sources: Participation plans; annual and semi-annual reports; MassHealth data; key informant interview transcripts
Instructions for Use of the Midpoint Review Form (HR-03201A)
Note: Year
LES Planned Activity Calculator & Tracker – Guidance and Midpoint Review for the Current LES Year
Subject: LES Planned Activity Calculator & Tracker – Guidance and Midpoint Review
Document Type: Internal communication and operational guidance
Organization: NHS Primary Care Practice Network
Programme: Local Enhanced Services (LES)
Related Programme: Long Term Conditions LES (LTC LES)
Purpose: Guidance for reviewing planned and actual LES activity and monitoring mid-year progress
Audience: GP practices and practice staff participating in LES programmes
Tools Referenced: Planned Activity Calculator & Tracker spreadsheet; BI spreadsheet on the intranet
Data Inputs: Practice weighted population; actual activity data from BI spreadsheet
Measurement Approach: Comparison of planned annual activity and recorded delivery with percentage achievement calculation
Special Notes: Only LTC LES includes a defined target; some LES programmes such as Care Homes LES are excluded from the calculator
Contract Period: Current LES contract year
Review Stage: Midpoint progress review
Future Actions: Distribution of individual LTC LES practice reports with predicted achievement and payment projections
Midpoint Performance Evaluation
Note: Year
Subject: Employee performance evaluation
Document Type: Performance evaluation form
Target Audience: Supervisors, employees
Endpoint Security Policy
Note: Document Owner
Procurement of an Endpoint Protection Solution with Maintenance and Support for JICS for Three Years
Year: 2025
Region / City: Centurion
Subject: Endpoint Protection Solution, ICT Infrastructure
Document Type: Bid Specification
Organization: Judicial Inspectorate for Correctional Services (JICS)
Author: SITA
Target Audience: Suppliers of Endpoint Protection Solutions
Effective Period: 3 years
Approval Date: 09 September 2025
Amendment Date: N/A
Supplemental Tables 1–5. Analyses of Factors Associated with Composite Complication Endpoint, Diagnostic Yield, and Therapeutic Consequences of in-ICU Transvenous Renal Biopsies
Number of patients: 80
Setting: Intensive care unit
Procedure: Transvenous renal biopsy
Study design: Observational analytical study
Statistical methods: Student’s t-test; Wilcoxon’s rank test; χ2 test; logistic regression with backward-stepwise variable elimination
Outcomes assessed: Composite complication endpoint; acute tubular necrosis diagnosis; diagnostic yield; in-ICU mortality; therapeutic consequences
Variables analyzed: Demographic characteristics; clinical scores (SOFA, SAPS II); laboratory parameters; anticoagulation and antiplatelet therapy; bleeding-risk factors; vasopressor use; mechanical ventilation; extracorporeal membrane oxygenation
Time comparison: TVRB performed before 2012 vs after 2012; biopsy after 2015
Therapeutic interventions evaluated: Corticosteroids; cyclophosphamide; plasmapheresis; intravenous immunoglobulins; rituximab; eculizumab; calcineurin inhibitors; anticoagulation
Definition of composite endpoint: Renal hematoma; macroscopic hematuria; transfusion during days 1–3 post-TVRB; SOFA score increase ≥1 point from TVRB day to day +3; hemoglobin decrease ≤ –2 g/dL from TVRB day to day +3
Curriculum Endpoint
Note: Year
Enterprise Endpoint Support Services (EESS) Scope Description
Note: Year
[iRTCW] Media capability enhancement for RTC endpoint
Year: 2025
Region / City: Online
Subject: Real-time communication, media capabilities, codec implementation
Document type: Change Request (CR)
Organization / Institution: 3GPP TSG-SA WG4
Author: NTT
Target audience: RTC system developers, network engineers
Work item code: iRTCW, TEI19
Release: Rel-19
Category: B (addition of feature)
Date of submission: 2025-07-14
Clauses affected: 16
Related specifications: TS 26.113, TS 26.114, TS 26.119, TS 24.229, TR 26.830
Revision: 1
Endpoint Security Policy
Year: [Insert Year]
Organization: [Insert Company Name]
Policy Type: Security Policy
Scope: All employees, contractors, consultants, temporaries, and affiliated third parties using endpoint devices
Responsible Department: IT Department
Author/Approver: Executive Team
Effective Date: [Insert Date]
Review Date: [Insert Date]
Version: [Insert Version Number]
Device Types Covered: Desktops, laptops, tablets, smartphones, personal devices (BYOD)
Security Measures: Encryption, MFA, Antivirus, Firewalls, Patching, Device Locking, Remote Access Controls, Backup, Monitoring, Incident Reporting
Compliance: Mandatory adherence by all users, enforcement actions for violations
Supplementary Table 1: Endpoint Definitions of Included Clinical Trials
Year: 2021-2024
Authors: Cabalag, Hofste, Morimoto, Ng, Ococks, Kelly, van den Ende, Veschoor, Wang, Yue
Endpoints: OS, PFS, pCR
Type of document: Supplementary table
Study type: Clinical trials
Definitions provided: Overall survival (OS), Progression-free survival (PFS), Pathological complete response (pCR)
Target population: Patients included in clinical trials
Data collection period: From randomization or treatment start to endpoints
Topics: AMFE Midpoint Endpoint