№ files_lp_3_process_7_071765
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Educational supervision and assessment guidance outlining the structure, requirements, evidence collection processes and accreditation framework for Unit 1.1 of a regional pharmacy workforce training programme in medicines optimisation.
Organisation:
Pharmacy Workforce Development South, University Hospitals Bristol and Weston NHS Foundation Trust
Address:
Marlborough Street, Bristol, BS2 8HW
Contact Telephone:
0117 342 6677
Email:
[email protected]
Website:
www.PWDS.nhs.uk
Programme Title:
Medicines Optimisation Training Programme for Pharmacy Support Staff
Unit:
Manage Patient Medication Requirements (Unit 1.1)
Document Type:
Educational Supervisor Guide
Version:
1.0
Publication Date:
January 2022
Subject Area:
Medicines optimisation, pharmacy practice, workforce development
Intended Audience:
Educational supervisors, programme support officers, pharmacy support staff trainees
Geographical Scope:
South West England
Associated Documents:
Medicines Optimisation Training Programme Handbook; assigned learning pathway; e-portfolio documentation
Assessment Methods:
Direct observation of practical skills (DOPS), competency-based assessments, accuracy logs, summative assessment interview
Issuing Body:
Pharmacy Workforce Development South
Price: 8 / 10 USD
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Note:
Year
Document Type:
Job Description
Organization:
Peabody
Year:
2022
Region / City:
Bristol
Topic:
Medicines Optimisation, Pharmacy Support
Document Type:
Training Programme
Institution:
University Hospitals Bristol and Weston NHS Foundation Trust
Author:
Pharmacy Workforce Development South (PWDS)
Target Audience:
Pharmacy Support Staff
Period of Validity:
Ongoing
Approval Date:
January 2022
Date of Changes:
None
Year:
2023
Region / city:
United Kingdom
Topic:
Medicines Optimisation, SGLT2 inhibitors
Document Type:
Protocol
Author:
NHS England
Target Audience:
Healthcare professionals, clinicians, systems involved in diabetes and heart failure treatment
Period of Validity:
Ongoing
Approval Date:
September 25, 2023
Date of Changes:
Not specified
Clinical Area:
Type 2 diabetes, heart failure, chronic kidney disease
Inclusion Criteria:
Patients aged 18 years and older prescribed empagliflozin, canagliflozin, ertugliflozin, or branded dapagliflozin for T2DM and/or HF
Exclusion Criteria:
Severe renal impairment, diabetic ketoacidosis, and other contraindications as per SPC
Background:
Dapagliflozin is now the first-line SGLT2i in England due to cost reduction following patent expiry.
Implementation Date:
Not specified
Post-switch:
No need for additional eGFR monitoring unless clinical concerns arise
Description:
Protocol outlining the process for switching eligible patients from other SGLT2 inhibitors to dapagliflozin for the management of Type 2 diabetes and heart failure in primary care.
Year:
2023
Region / city:
United Kingdom
Topic:
Medicines optimisation, SGLT2 inhibitors, diabetes, heart failure
Document type:
Protocol
Organ / institution:
NHS England
Author:
NHS
Target audience:
Clinicians, healthcare providers
Period of validity:
Ongoing
Approval date:
Not specified
Modification date:
Not specified
Document Type:
Supplementary application form
Related Form:
Case for Support
Submission System:
Je-S
Guidance Reference:
DPFS Guidance for Applicants
Purpose:
Assessment of proposals for hit to lead, lead optimisation and candidate selection funding
Confidentiality:
Information treated in strict confidence and reviewed under confidentiality agreements
Intended Users:
Applicants seeking funding
Reviewing Body:
Panel Members and External Peer Reviewers
Project Information Required:
Principal Investigator, Institution, Project Title
Scientific Scope:
Target Product Profile and Investigational New Drug parameters
Data Requirements:
Chemical structures, biological assays, physicochemical properties, DMPK, toxicology, in vivo studies
Word Limits:
20 words per TPP field; 300 words per tractability section
Organisation:
West Midlands Cancer Alliance
Programme:
MDT Optimisation Programme
Programme Manager:
Marie-Claire Wigley
Contact:
[email protected]
Region:
West Midlands
Sector:
Cancer care services
Focus:
Multi-Disciplinary Teams (MDTs)
Objectives:
Workforce development, leadership development, peer review reinstatement, treatment variation reduction
Key Activities:
MDT Coordinator Forum, Leadership Development Webinars, Peer Review Process
Target Audience:
Core clinical MDT members including Chairs, Deputy Chairs, Clinical Nurse Specialists, Allied Health Professionals, Radiologists, Oncologists, MDT Coordinators
Webinar Period:
June to October 2025
Follow-up Session:
Four months after October 2025
Next MDT Coordinator Forum Date:
3 July 2025
Quality Assurance Context:
Resumption of SSQD data collection and local peer review visits
Related Programme:
Specialised Services Quality Dashboard (SSQD)
Year:
2023
Region / city:
United Kingdom
Topic:
Medicine optimisation, diabetes, heart failure, chronic kidney disease
Document type:
Protocol
Organisation:
NHS England
Author:
Not specified
Target audience:
Healthcare professionals
Period of validity:
Ongoing
Approval date:
September 25, 2023
Modification date:
Not specified
Clinical condition:
Type 2 diabetes mellitus, heart failure, chronic kidney disease
Medication:
Dapagliflozin, Empagliflozin, Canagliflozin, Ertugliflozin
Intended use:
Generic dapagliflozin
Switch criteria:
Based on patient needs and clinical appropriateness
Inclusion criteria:
Patients aged 18 years and older currently prescribed certain SGLT2 inhibitors
Exclusion criteria:
History of adverse reactions or specific clinical conditions
Recommended dosage:
10mg once daily, with adjustments for hepatic or renal impairment
Monitoring:
HbA1c, blood tests, signs of infections or DKA
Drug interactions:
Fewer interactions compared to other SGLT2 inhibitors
Patient communication:
Information leaflets, SMS, letters
Post-switch monitoring:
Routine HbA1c checks, watch for DKA
Clinical recommendation:
Consider shared decision-making and patient discussions
References:
NICE guidelines, NHS guidance, formulary recommendations
Tender number:
LPMAT00120GX
Issue date:
25/03/2025
Closing date and time:
16/04/2025 at 14h00
Tender validity period:
180 days from the closing date and time
Clarification meeting:
Date: 03 April 2025 Time: 10H00 Venue: MS teams
Tender office:
Matimba Main Security Gate Matimba Power Station Nelson Mandela Drive Lephalale0555
Date of Issue:
25/03/2025
Contract Duration:
5 years
Region:
Lephalale
Industry:
Energy
Document Type:
Invitation to Tender
Organisation:
Eskom Holdings SOC Ltd
Target Audience:
Suppliers, Contractors
Validity Period:
180 days
Note:
Clarification Meeting
03 April 2025
Eskom Representative:
Azwifaneli Fanie Thagwana
Scope of Work:
Supply, delivery, offloading and optimisation of chemicals
Tax Requirements:
PAYE
Local Content Declaration:
Required
Year:
2019
Region / City:
United Kingdom
Theme:
Healthcare, Defence
Document Type:
Announcement
Organization:
Ministry of Defence
Author:
Defence Healthcare Delivery Optimisation Programme
Target Audience:
Healthcare providers, Defence sector professionals
Period of Validity:
April 2019 - April 2020
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
Not specified
Country:
Australia
Sector:
Forest and Wood Products
Training Package:
FWP Forest and Wood Products Training Package Version 5.0
Unit Code:
FWPCOT3XXX
Unit Title:
Apply principles of timber and process optimisation in sawmill operations
Unit Sector Code:
COT
Document Type:
Unit of competency and assessment requirements
Prerequisite Unit:
Nil
Regulatory Status:
No occupational licensing, legislative or certification requirements at time of publication
Subject:
Timber optimisation and material flow optimisation in sawmilling operations
Key Topics:
timber value and volume recovery; workflow optimisation; optimisation drivers; equipment performance; optimisation initiatives
Industry Context:
Sawmill operations and forest product manufacturing
Technologies Referenced:
3D scanning; X-ray scanning devices; acoustic scanning devices; automated transfer systems; computer-assisted machine centres for sawing and re-sawing
Work Areas Mentioned:
log sorting; green mill sawing; dry mill processing; grading; timber treatment
Assessment Environment:
Forest product factory setting or simulated workplace conditions
Assessment Components:
Performance Evidence; Knowledge Evidence; Assessment Conditions; Foundation Skills
Related Resource:
VETNet Companion Volumes and Implementation Guides
Year:
2016
Region / City:
N/A
Topic:
Performance Optimization, Back Test Comparison
Document Type:
Technical Report
Organization / Institution:
N/A
Author:
N/A
Target Audience:
N/A
Period of Validity:
Oct to Dec 2016
Approval Date:
N/A
Date of Changes:
N/A
Year:
2024
Region / City:
Lancashire and South Cumbria
Topic:
Asthma Management
Document Type:
Standard Operating Procedure
Organization:
NHS
Author:
Unknown
Target Audience:
Healthcare professionals, particularly those involved in asthma management
Action Period:
Ongoing
Approval Date:
November 2024
Modification Date:
None
Year:
2023
Region / city:
Australia
Subject:
Pharmaceutical compounding guidelines
Document Type:
Guideline
Organization / Institution:
Pharmacy Board of Australia
Author:
Pharmacy Board of Australia
Target Audience:
Registered pharmacists, education providers, employers
Period of validity:
Indefinite
Approval Date:
Not specified
Date of amendments:
Not specified
Year:
2016
Region / City:
Australia
Topic:
Pharmacy, Medicine Compounding
Document Type:
Consultation Response
Organization:
Pharmaceutical Society of Australia
Author:
Dr Lance Emerson, Chief Executive Officer
Target Audience:
Pharmacists, Pharmacy Regulators
Period of Validity:
Indefinite
Approval Date:
1 February 2016
Date of Amendments:
None
Contextual Description:
Document is a public consultation response discussing terminology issues and proposed updates regarding compounded parenteral medicines, primarily aimed at Australian pharmacists.
Organisation:
Canberra Health Services
Document type:
Guideline
Reference number:
CHS25/225
Jurisdiction:
Australian Capital Territory
Healthcare setting:
Public health services
Subject area:
Medication management
Professional scope:
Nursing and midwifery practice
Approved by:
Drug and Therapeutics Committee
Target professionals:
Registered nurses and registered midwives
Patient groups:
Adults, children 12 years or older, and selected medicines for children under 12 years
Exclusions:
Neonates, Special Care Nursery patients, Neonatal Intensive Care Unit patients
Regulatory framework:
Australian medicines scheduling (Schedules 2, 3, 4, and 8)
Content components:
Governance, safe use, documentation, approved medicine lists
Year:
2023
Region / city:
European Union
Topic:
Pharmaceutical technology development
Document type:
Briefing document
Organization:
European Medicines Agency
Author:
Not specified
Target audience:
Pharmaceutical experts, regulatory authorities
Period of validity:
Not specified
Approval date:
Not specified
Date of modifications:
Not specified
This document is a briefing source for discussing pharmaceutical technology and regulatory aspects at a QIG 1:
1 meeting.
Year:
2023
Country:
Australia
Topic:
Opioid dependence treatment
Document type:
Information overview
Program:
ODT Community Pharmacy Program
Administering body:
Pharmacy Programs Administrator
Related scheme:
Pharmaceutical Benefits Scheme
Legislative framework:
National Health (Highly specialised drugs program) Special Arrangement 2021
Target audience:
Community pharmacists and hospital pharmacists
Effective date:
1 July 2023
Funding period:
2023–24 to 2026–27
Medicines covered:
Methadone, buprenorphine, buprenorphine with naloxone
Regulatory classification:
Schedule 8 controlled drugs
Source type:
Government health program guidance
Document type:
Q&A guidance
Jurisdiction:
Japan
Subject:
Import and shipment of medicines and medical devices
Issuing authority:
Ministry of Health, Labour and Welfare
Intended users:
Individuals importing or sending medicines for personal use
Scope:
Prescription medicines, injections, syringes, and medical devices
Import purpose:
Personal use
Regulatory framework:
Pharmaceutical and Medical Device regulations
Application system:
Online Import Confirmation system
Related forms:
Import Confirmation Application Form (Form 12); Explanation of Pharmaceutical Product (Form 13)
Year:
2024
Region / city:
Denmark
Topic:
Medicine, Health Economics
Document type:
Template
Organization / institution:
Danish Medicines Council
Author:
Danish Medicines Council
Target audience:
Pharmaceutical companies
Period of validity:
Ongoing
Approval date:
10 September 2024
Date of changes:
1 April 2025
Version:
2.5