№ files_lp_4_process_2_37704
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This document is a formal proposal outlining the discontinuation of a course/program and associated actions within an academic institution.
Year:
2013
Region / City:
N/A
Topic:
Program Discontinuation
Document Type:
Proposal
Institution:
School of Business and Technology
Author:
Andrew Blitz
Target Audience:
Faculty, Academic Affairs
Action Period:
Fall 2014
Approval Date:
12/31/2013
Change Date:
02/18/2014
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Year:
2026
Region / City:
Long Beach, CA
Theme:
Higher education, curriculum changes
Document Type:
Proposal form
Institution:
California State University, Long Beach
Author:
College of Education
Target Audience:
Faculty members, academic departments, program coordinators
Period of Action:
2026-2027 academic year
Approval Date:
Pending
Date of Changes:
N/A
Year:
2026
Region / City:
Long Beach, California
Topic:
Curriculum Change
Document Type:
Proposal
Organization / Institution:
California State University, Long Beach
Author:
Faculty members
Target Audience:
Faculty, program coordinators, academic administrators
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Amendments:
Not specified
Note:
Year
Topic:
Program Discontinuation
Document Type:
Form
Organization / Institution:
ACCSC
Target Audience:
Educational institutions
Year:
2026
Region / City:
United Kingdom
Theme:
Pharmaceutical Treatment
Document Type:
Prescribing Information
Organization:
NHS
Author:
Dr. Joanne Ritchie
Target Audience:
Healthcare professionals, specifically specialists and GPs
Period of Validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Contraindications:
Venous thromboembolic disorder, arterial thromboembolic disease, known thrombophilic disorders, known osteoporosis, headaches with focal neurological symptoms, pregnancy, breastfeeding
Monitoring:
DEXA scan recommended after 1 year of treatment
Special Warnings/Precautions:
Use of non-hormonal contraception for at least 1 month after initiation
Adverse Effects:
Hot flushes, headache
Primary Care responsibilities for continuation:
Prescribe as recommended, seek advice from the specialist if needed
Specialist Service responsibilities for initiation:
Discuss benefits and side effects with the patient, initiate treatment and monitor
Criteria for Discontinuation:
Menopause, increase in migraine frequency, ATE/VTE events, acute liver deterioration
Date of Initiation:
Not specified
Communication:
Contact details for the specialist and hospital pharmacy provided
Note:
Year
Subject:
Discontinuation of Appointment
Document Type:
Notice
Organization / Institution:
Washington State University
Target Audience:
Employee
Year:
2017
Region / City:
Pullman, Washington
Subject:
Employment termination
Document Type:
Notification
Organization / Institution:
Washington State University
Author:
Appointing Authority
Target Audience:
Employee of Washington State University
Effective Period:
April 3, 2017
Approval Date:
April 3, 2017
Amendment Date:
None
Year:
2024
Note:
Region / City
Theme:
Product Discontinuation
Document Type:
Notice
Organization / Institution:
Honeywell
Author:
Honeywell Intelligrated
Period of Validity:
2024-2025
Final Order Date:
6-09-2025
Discontinuation Date:
8-09-2025
Date:
May 15, 2024
Company:
Honeywell Intelligrated
Legal Entity:
Intelligrated Systems, LLC
Product Name:
Mathews SWD (Swivel Wheel Divert)
Subject:
Discontinuation of product line and last time buy notice
Discontinuation Date:
August 23, 2025
Final Order Date (Last Time Buy):
June 23, 2025
Reason for Discontinuation:
Supply chain and component obsolescence constraints
Replacement Product:
Intelligrated Wheel Divert 2.0
Affected Materials:
Multiple part numbers listed in Mathews SWD Table 1.pdf
Order Conditions:
Non-cancellable and non-returnable LTB orders; first come, first served basis
Warranty Terms:
No warranty replacement parts available after discontinuation
Support Termination:
All parts and service support cease on August 23, 2025
Contact Information:
Parts Hotline 877.315.3400 (Option 2); [email protected]
Intended Audience:
Customers and purchasers of Mathews SWD products
Year:
2023
Region / City:
United States
Subject:
Healthcare, Pharmaceutical, Respiratory Care
Document Type:
Notification, Regulatory Update
Organization:
GlaxoSmithKline (GSK), U.S. Food and Drug Administration (FDA), MassHealth
Author:
GlaxoSmithKline (GSK), MassHealth
Target Audience:
Healthcare providers, MassHealth members, Pharmacists
Effective Date:
December 31, 2023 (discontinuation), December 4, 2023 (PA changes)
Date of Approval:
June 2, 2023
Date of Changes:
September 29, 2023
Year:
2019
Region / City:
United States
Topic:
Affordable Care Act, Health Insurance
Document Type:
Regulatory Guidance
Agency / Institution:
U.S. Department of Health and Human Services
Author:
Centers for Medicare & Medicaid Services
Target Audience:
Health Insurance Issuers, Exchanges, Consumers
Effective Period:
2019 and Beyond
Approval Date:
July 6, 2018
Modification Date:
July 30, 2019
Document type:
Administrative form
Subject:
Course discontinuation and withdrawal from delivery
Institutional context:
Higher education
Responsible unit:
Quality team
Institutional body for approval:
Portfolio Oversight Committee
Institutional authority supporting proposal:
Dean of School / Head of Higher Education
Fields included:
Course name and award; School or Partner Institution; Course Leader; Validation period; Rationale for discontinuation; Student numbers; Student consultation; Exit strategy; Closure timeline; Applicant actions; Implications for other courses; Staffing implications
Student data scope:
Previous three academic years including headcount and FTE for part-time students
Academic levels referenced:
Level 3; Level 4; Level 5; Level 6; Level 7
Submission requirement:
Form submitted to Quality team for allocation of form number at least 10 working days before committee consideration
Approval process:
Signature and date by School authority and Portfolio Oversight Committee
Purpose:
Formal proposal and review process for permanent withdrawal of an academic course
Country:
United States
State:
Illinois
City:
Chicago
Subject:
Discontinuation of a hospital facility
Document type:
Legal notice of public hearing
Related legislation:
Illinois Health Facilities Planning Act
Regulatory reference:
77 Illinois Administrative Code Part 1130
Responsible body:
Illinois Health Facilities and Services Review Board
Project number:
25-002
Healthcare facility:
Advocate Trinity Hospital
Facility address:
2320 East 93rd Street, Chicago, Illinois
Public hearing date:
April 7, 2025
Public hearing time:
1:00 PM
Hearing location:
Compassion Baptist Church, 2650 E 95th St, Chicago, IL 60617
Participation format:
Public hearing with written and verbal comments
Submission requirements:
Two copies of supporting documentation on 8½ × 11 inch paper
Contact person:
John P. Kniery
Contact phone:
(217) 782-3516
TTY contact:
800-547-0466
Accessibility notice:
Meeting accessible to persons with special needs upon prior notification
Year:
2023
Region / City:
Not specified
Topic:
Biologic persistence analysis
Document Type:
Research Supplement
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers, Healthcare Professionals
Period of Effect:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Region / City:
N/A
Subject:
Product discontinuation, replacement product
Document Type:
Announcement
Organization / Institution:
AccuTec, Inc.
Author:
Garnett A. Andes
Target Audience:
Existing customers
Effective Date:
January 20, 2025
Date of Change:
January 20, 2025
Year:
2026
Region / City:
Not specified
Topic:
Pediatric endocrinology, growth hormone therapy
Document Type:
Clinical trial information letter
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Parents and guardians of children with isolated growth hormone deficiency
Study Type:
Non-inferiority randomized controlled trial
Purpose:
To evaluate the final height outcomes in children with I-GHD after discontinuation vs continuation of GH therapy
Participation:
Voluntary
Method:
GH stimulation test
Year:
2025
Region / City:
Washington, D.C.
Topic:
Drug Development, Clinical Trials, Sickle Cell Disease
Document Type:
Press Release
Organization / Institution:
Sickle Cell Medical Advocacy Inc., Sickle Cell Foundation of Georgia, Inc., Sickle Cell Disease Association of America Inc., Crescent Foundation, SC RED, Sickle Cell 101, Sickle Cell Community Consortium
Author:
Sickle Cell Advocates
Target Audience:
Sickle Cell Disease Community, Medical Researchers, Pharmaceutical Industry
Effective Period:
August 15, 2025
Approval Date:
August 15, 2025
Date of Changes:
N/A
Note:
Contextual Description
Date:
[Date]
Country:
United States
State:
Washington
Topic:
Health insurance coverage and plan enrollment
Document type:
Notice letter
Issuing organization:
Washington Healthplanfinder (Washington Health Benefit Exchange) and participating health plan issuer
Recipient:
Policyholder and enrolled household members
Subject:
Termination of current health plan and selection of replacement coverage
Current coverage end date:
December 31, [insert current year]
Open enrollment period:
November 1 – December 15, [insert current year]
Additional plan selection period:
December 16, [insert current year] – January 15, [insert upcoming year]
New coverage start dates:
January 1, [insert upcoming year] or February 1, [insert upcoming year] depending on enrollment date
Related programs:
Cascade Care Savings Program, Premium Tax Credits
Contact platform:
Washington Healthplanfinder (www.wahealthplanfinder.org
Note:
)
Note:
Year
Topic:
ICT Products and Services
Document Type:
Order Form
Note:
Year
Year:
2006
Region / City:
Australian Capital Territory
Subject:
Legal procedures, subpoena
Document Type:
Court Form
Issuing Authority:
Court of the Australian Capital Territory
Author:
Not specified
Target Audience:
Legal professionals, defendants, plaintiffs
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A