№ files_lp_3_process_7_093931
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This letter outlines the requirements and procedures for completing the Annual Safety & Health Management System Review for SHARP work sites, emphasizing the importance of maintaining a safe work environment and meeting OSHA standards.
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
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2011
Region / City:
City of _______
Subject:
Construction, Environmental Protection
Document Type:
Ordinance
Organization / Institution:
City Council of _______
Author:
City Council
Target Audience:
Contractors, City Employees
Period of Validity:
Effective upon passage
Approval Date:
[Insert Effective Date]
Date of Changes:
[Insert Effective Date]
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:
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
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:
2021
Region / City:
Canberra
Topic:
Medication Safety
Document Type:
Policy Statement
Organization / Institution:
Canberra Health Services
Author:
Not specified
Target Audience:
CHS staff, including employees, contractors, volunteers, and students
Effective Period:
Indefinite
Approval Date:
12/05/2021
Amendment Date:
12/05/2021
Date:
April 20, 2016
Location:
Ontario County, New York, USA
Type of document:
Meeting minutes
Organization:
Ontario County Traffic Safety Board (TSB)
Participants:
Board members, TSB partners, guests
Topics discussed:
Board membership changes, mission statement, traffic safety initiatives, public service announcements, funding requests, law enforcement updates, youth programs, safety campaigns, upcoming events
Programs mentioned:
STOP-DWI, R.E.A.L. CHOICES, No Empty Chair, Safe Stop, Click it or Ticket
Incidents reported:
DWI arrests, distracted driving fatalities, underage drinking, drug possession
Next meeting:
August 10, 2016
Year:
2019
Region / City:
Oxford
Topic:
Health and Safety
Document Type:
Safety Update
Organization:
University of Oxford, Department of Materials
Author:
Linda Curson
Target Audience:
Staff, visitors, students
Period of Validity:
Ongoing
Approval Date:
25 March 2019
Date:
December 12, 2018
Type of document:
Meeting minutes
Organization:
Ontario County Traffic Safety Board
Location:
Ontario County, New York, USA
Attendees:
Board members, TSB partners, and guests listed in document
Topics discussed:
Board member resignations, appointments, traffic safety programs, overdose audits, sobriety checkpoints, new online driver courses, and public safety initiatives
Next meeting:
February 13, 2019