№ files_lp_3_process_7_093932
File format: docx
Character count: 24760
File size: 92 KB
The document outlines the application process for the SHARP Program, detailing the required steps for submitting a funding application for supportive housing development under the American Rescue Plan.
Year:
2023
Region / City:
North Carolina
Theme:
Housing Finance, Supportive Housing
Document Type:
Application Form
Organization:
North Carolina Housing Finance Agency (NCHFA)
Author:
NCHFA
Target Audience:
Housing developers, nonprofit organizations, local governments
Period of Validity:
Until July 21, 2023
Approval Date:
July 21, 2023
Date of Modifications:
N/A
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2022
Region / City:
Australia
Topic:
Medical treatment approval and submission for pembrolizumab and lenvatinib
Document type:
Submission for drug listing
Organization / Institution:
Pharmaceutical Benefits Advisory Committee (PBAC), Therapeutic Goods Administration (TGA)
Author:
Merck Sharp & Dohme (Australia) Pty Ltd
Target audience:
Medical professionals, health regulators
Period of validity:
2022 onward
Approval date:
August 10, 2021
Amendment date:
Not specified
Year:
2023
Region / City:
Australia
Theme:
Oncology, Pharmaceutical
Document Type:
Submission
Organization / Institution:
Merck Sharp & Dohme (Australia) Pty Ltd
Author:
Not specified
Target Audience:
Medical professionals, policymakers
Period of Effectiveness:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / City:
Australia
Subject:
Oncology / Colorectal Cancer Treatment
Document Type:
Medical submission
Agency / Organization:
Pharmaceutical Benefits Advisory Committee (PBAC)
Author:
Not specified
Target Audience:
Medical practitioners
Effective Period:
Ongoing
Approval Date:
Not provided
Date of Revision:
Not provided
Year:
2024
Region / City:
Australia
Topic:
Oncology / Cancer Treatment
Document Type:
Pharmaceutical Submission
Organization:
Merck Sharp & Dohme
Author:
Merck Sharp & Dohme
Target Audience:
Healthcare professionals, regulatory bodies, pharmaceutical industry
Effective Period:
From September 2024
Approval Date:
Pending
Date of Changes:
September 2024
Context:
A submission by Merck Sharp & Dohme to request a multi-indication listing for pembrolizumab to treat advanced or metastatic cancers under the Pharmaceutical Benefits Scheme in Australia.
Year:
2022
Region / City:
Australia
Theme:
Oncology, Pharmacology
Document Type:
Addendum
Organ / Institution:
Merck Sharp & Dohme (Australia) Pty Ltd
Author:
Not specified
Target Audience:
Healthcare professionals, regulatory bodies
Period of Validity:
Indication approved on February 7, 2022
Approval Date:
07 February 2022
Change Date:
Not specified
Year:
2022
Region / city:
Australia
Topic:
Early-stage triple negative breast cancer treatment
Document type:
Pharmaceutical submission
Organization / institution:
Merck Sharp & Dohme (Australia) Pty Ltd
Author:
Not specified
Target audience:
Medical professionals, healthcare providers
Effective period:
From September 2022
Approval date:
2 September 2022
Modification date:
Not specified
Registration status:
Approved by TGA
Background:
Pembrolizumab was approved by the TGA for the treatment of early-stage triple-negative breast cancer in combination with chemotherapy as neoadjuvant treatment and as monotherapy post-surgery.
Condition:
Triple negative breast cancer
Indication:
Early stage triple negative breast cancer
Restriction:
Section 100 (Efficient funding of chemotherapy), Authority Required – Streamlined
Treatment initiation criteria:
Hormone receptor negative, HER2 negative, preparing for surgery, ECOG status 1 or less, treatment combined with chemotherapy, no previous treatment, not exceeding 24 weeks of therapy
Continuation criteria:
Must have undergone surgery, ECOG status 1 or less, monotherapy for adjuvant phase, no more than 27 weeks of therapy
Grandfathering criteria:
Must have previously received non-PBS subsidised treatment
Price:
$7,881.87 private, $7,733.78 public for neoadjuvant; private and public prices for adjuvant not specified
Number of doses:
7 for neoadjuvant, 8 for adjuvant
Source:
Table 1.1-1, pp12-14
Context description:
A pharmaceutical submission for the approval of pembrolizumab as a treatment for early-stage triple-negative breast cancer, including neoadjuvant and adjuvant therapy details and pricing for PBS listing.
Year:
2021
Region / City:
Australia
Topic:
Pneumococcal vaccine submission
Document type:
Submission for listing on the National Immunisation Program
Author:
Merck Sharp & Dohme (Australia) Pty Ltd
Target audience:
Health professionals, regulatory bodies, policy makers
Period of validity:
Ongoing
Approval date:
16 July 2021 (FDA approval), 14 October 2021 (EMA recommendation)
Date of changes:
Not specified
Context:
A clinical submission for the inclusion of a 15-valent pneumococcal conjugate vaccine (PCV15) on the National Immunisation Program for adults at risk of pneumococcal disease.
Year:
2017
Region / city:
Australia
Theme:
Oncology, Immunotherapy
Document type:
Pharmaceutical Submission
Organization / Institution:
Merck Sharp & Dohme (Australia) Pty Ltd
Author:
Merck Sharp & Dohme
Target audience:
Healthcare professionals, medical practitioners
Effective period:
Ongoing
Approval date:
March 2017
Changes date:
Not specified
Context:
A pharmaceutical submission for the listing of pembrolizumab for the first-line treatment of metastatic non-small cell lung cancer (NSCLC) patients, detailing proposed PBS listings, treatment phases, and clinical criteria.
Date:
Friday 16th June
Location:
Cadder Community Centre, Glasgow, Scotland
Event Type:
One-day members conference
Organizer:
Glasgow and West of Scotland Forum (GWSF)
Participants:
CCHAs, community members, policy advisors
Speakers:
Peter Howden, Colleen Rowan, David Cowan, Francis Stuart, Maureen Cope, Sandy Campbell, Fraser Stewart, David Bookbinder
Sessions:
Plenary talks, café sessions, networking
Topics:
Poverty reduction, community development, youth employment, succession planning
Booking Contact:
Eleanor McCormack
Email:
[email protected]
Year:
2023
Region / city:
Australia
Topic:
Pneumococcal vaccination
Document type:
Submission
Agency / organization:
Australian Technical Advisory Group on Immunisation (ATAGI)
Author:
Merck Sharp & Dohme (Australia) Pty Ltd
Target audience:
Healthcare professionals involved in immunization
Period of validity:
Not specified
Approval date:
Expected by 30 April 2023
Date of changes:
9 February 2023
Year:
2022
Region / City:
North Carolina
Topic:
Occupational Health and Safety
Document Type:
Government Letter
Organization / Institution:
North Carolina Department of Labor
Author:
Kevin O’Barr
Target Audience:
SHARP Employers in North Carolina
Period of Action:
2022
Approval Date:
January 5, 2022
Modification Date:
N/A
Year:
N/A
Region / City:
N/A
Theme:
History, English Monarchs
Document Type:
Exercise
Author:
N/A
Target Audience:
Students of English, History
Validity Period:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Bezlotoxumab, Solution concentrate for I.V. infusion 1000 mg in 40 mL,Zinplava®, Merck Sharp & Dohme
Year:
2021
Region / City:
Australia
Topic:
Pharmaceutical Approval
Document Type:
Resubmission Request
Author:
Merck Sharp & Dohme
Target Audience:
Medical Practitioners, Healthcare Professionals
Period of Validity:
Not specified
Approval Date:
8 November 2017
Date of Changes:
November 2017
Treatment Phase:
Initial
Indication:
Clostridium Difficile Infection (CDI)
Restriction Level:
Section 100 – Authority Required
Prescriber Type:
Dental, Medical Practitioners, Nurse Practitioners, Optometrists, Midwives
Clinical Criteria:
Confirmed Toxin B Positive CDI, High Risk of Recurrence
Clinical Claim:
Bezlotoxumab more effective than SoC antibiotics in preventing CDI recurrence
Cost Effectiveness:
Comparison with Standard of Care (SoC)
Background:
TGA approved on 8 November 2017 for prevention of CDI recurrence
Context:
Pharmaceutical resubmission seeking authority for listing bezlotoxumab as an option for preventing Clostridium Difficile Infection recurrence in patients at high risk, emphasizing its cost-effectiveness over standard antibiotic treatments.
Year:
2015
Region / City:
Rensselaer, NY; Boston, MA
Document Type:
Audit Report
Facility Type:
Juvenile Detention and Transition Facility
Agency:
Massachusetts Department of Youth Services
Auditor:
Kurt Pfisterer
Facility Name:
Westboro Sharp Building
Number of Beds:
27
Date of On-Site Audit:
April 8, 2015
Audit Period:
April 8, 2014 – April 8, 2015
Facility Programs:
Westboro Reception Unit, Sharp Transition Program
Youth Population:
Male adolescents aged 12–21
PREA Coordinator:
Monica King
Executive Officer:
Peter Forbes
Security Level:
Hardware-secure
Observations:
Video surveillance coverage, staff-to-youth ratio, private interviews, structured programming, clinical and educational services
Year:
2018
Region / city:
Australia
Subject:
Pharmaceutical application for diabetes treatment
Document type:
Pharmaceutical submission
Organization / institution:
PBAC, TGA
Author:
Merck Sharp & Dohme (Australia) Pty Ltd
Target audience:
Medical practitioners, healthcare professionals
Validity period:
Ongoing since 2018
Approval date:
16 April 2018
Revision date:
March 2018
Year:
2023
Region / City:
United States
Topic:
Emergency Housing Assistance for Veterans
Document Type:
Program Guidelines
Organization:
U.S. Department of Veterans Affairs
Author:
U.S. Department of Veterans Affairs
Target Audience:
Veterans, SSVF Grantees, VA and community partners
Effective Period:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Project Name:
[Project Name]
Recipient/Subrecipient:
[Agency Legal Name]
Component Type:
TH / RRH / PSH / SSO or SSO–SO
Type of Document:
Supportive services agreement
Program Framework:
Continuum of Care (CoC)
Regulatory References:
24 CFR 578.75(h); FY2025 CoC NOFO
Participants:
Housing program participants
Services Covered:
Housing-focused supportive services
Data System:
HMIS or comparable database
Participant Rights:
Non-discrimination, confidentiality, grievance process
Agreement Term:
Effective [Start Date] through [End Date] or while enrolled in the project
Signatories:
Participant; Project staff representative
Year:
2025
Region / City:
New Jersey
Theme:
Family Support Services, Child Welfare
Document Type:
Contract Guidelines
Organization / Institution:
Department of Children and Families (DCF)
Author:
Department of Children and Families (DCF)
Target Audience:
Contractors, Service Providers
Period of Validity:
From July 1, 2025
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2018
Region / City:
Minnesota
Theme:
Supportive Housing, Homelessness Assistance
Document Type:
Policy Change Notice
Organization:
Minnesota Housing
Author:
Minnesota Housing
Target Audience:
Housing providers, Coordinated Entry system managers
Effective Date:
January 1, 2019
Change Date:
2018
Period of Application:
2018-2019