№ lp_1_34082
File format: docx
Character count: 6099
File size: 18 KB
This document provides guidelines on informed consent for injections, outlining the importance of patient understanding of risks and side effects, with specific reference to corticosteroid injections.
Year:
2023
Region / city:
UK
Topic:
Medical procedures, Informed consent, Physiotherapy
Document type:
Guidelines
Author:
Chartered Society of Physiotherapists
Target audience:
Healthcare professionals, Physiotherapists
Date of approval:
2023
Date of changes:
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:
2020
Region / city:
Australia
Topic:
Biosimilar medicine submission
Document type:
Pharmaceutical submission
Organization / institution:
Pharmaceutical Benefits Advisory Committee (PBAC)
Author:
Maxx Pharma Pty Ltd
Target audience:
Healthcare professionals, regulatory bodies
Period of validity:
Ongoing
Approval date:
November 2022
Modification date:
November 2022
Note:
Year
Topic:
Lipid disorders, Cardiovascular Risk
Document Type:
Medical guideline
Target Audience:
Medical professionals, healthcare providers
Year:
2022
Region / City:
ACT and surrounding NSW
Topic:
Paediatric Diabetes Care, Insulin Pump Therapy
Document Type:
Clinical Guideline
Organization:
Canberra Health Services (CHS)
Author:
Canberra Health Services, Paediatric Endocrinology and Diabetes Service
Target Audience:
Paediatric Diabetes Healthcare Providers
Period of Validity:
N/A
Approval Date:
N/A
Date of Last Revision:
N/A
Version number:
6.0
Approved by:
Medicines Committee
Ratified by:
Medicines Committee
Date ratified:
June 2023
Original author:
Luton & Bedfordshire Lead Pharmacist
Executive Director lead:
Chief Medical Officer
Implementation Date:
July 2023
Last Review Date:
June 2023
Next Review Date:
June 2026
Services:
Trustwide, Mental Health and LD, Community Health Services
Type of document:
Policy
Scope:
Long-acting antipsychotic injections, typical and atypical
Target audience:
Clinicians, pharmacists, mental health services staff
Document structure:
Includes guidance on initiation, choice, and monitoring of depot injections, adverse effect reporting, and appendices with forms and rating scales
Year:
2016
Region / City:
United States
Topic:
Ophthalmology, Risk Management
Document Type:
Risk Management Recommendations
Organization / Institution:
OMIC
Author:
Anne M. Menke, Pauline Merrill, Trexler M. Topping, George Williams
Target Audience:
Ophthalmologists, Healthcare Providers
Period of Validity:
Not specified
Approval Date:
8/26/16
Date of Changes:
Not specified
Year:
2019
Region / City:
New Delhi, India
Sector:
Energy
Document Type:
Request for Qualification
Organization:
REC Transmission Projects Company Ltd.
Author:
REC Transmission Projects Company Ltd.
Target Audience:
Potential Bidders for Transmission Service Provider
Period of Validity:
Until 08.02.2019
Approval Date:
12th January 2019
Amendments Date:
Not provided
Organisation:
Hope Vets
Address:
Shantock Hall Lane, Bovingdon, HP3 0NQ
Telephone:
01442 833198
Email:
[email protected]
Website:
www.hopevets.com
Document type:
Instructional handout
Subject:
Administration of subcutaneous injections in pets
Medications mentioned:
Cytopoint, Librela, Solensia, Zycortal, insulin
Intended audience:
Pet owners administering injections at home
Related resources:
YouTube videos; Caninsulin website
Sharps disposal guidance:
Return to veterinary practice; use of sharps container or sealed container
Year:
2025
Region / City:
England
Subject:
Healthcare / NHS
Document Type:
Official communication
Organization / Institution:
NHS England
Author:
Erika Sutcliffe
Target Audience:
Healthcare professionals involved in NHS primary care
Effective Period:
From 1st May 2025
Approval Date:
28th May 2025
Date of Changes:
28th May 2025
Year:
2015
Region / Institution:
United Kingdom, Royal College of Radiologists
Subject:
Patient safety and documentation in intra-articular injections
Document type:
Audit report
Authors:
Dr Andrew Koo, Dr Daniel Fascia; Updated by P Mehrotra (2018), D Remedios (2022)
Target audience:
Radiologists, clinical staff performing joint injections
Review date:
23 July 2022
Publication date:
24 June 2015
Indicators:
Documentation of type, volume, and concentration of local anaesthetic agents
Methodology:
Collection of patient data from RIS, adherence to WHO and RCR safety guidelines
Recommendations:
Use of WHO checklist, departmental guidelines, and report macros for documentation
Year:
2026
Region / City:
Louisiana, Baton Rouge
Subject:
Procurement of Hydroxocobalamin Injections
Document Type:
Invitation to Bid / Procurement Terms
Agency:
Louisiana Department of Health, Office of State Procurement
RFx Number:
3000025811
Bid Submission Deadline:
03/04/2026 @ 10:00 A.M. (Central Time)
Inquiry Deadline:
02/18/2026
Response to Inquiries Deadline:
02/25/2026
Delivery Instructions:
Physical or online submission to Office of State Procurement
Payment Terms:
Unit price compensation, full delivery not required for partial payment
Authorized Contact:
Alex Jackson
Website for Registration:
https://lagoverpvendor.doa.louisiana.gov/irj/portal/anonymous?guest_user=self_reg
Online Bid Portal:
LaPAC
Year:
2022
Region / city:
N/A
Subject:
Platelet rich plasma (PRP) therapy
Document type:
Clinical guideline
Institution:
HERC
Author:
N/A
Target audience:
Healthcare professionals, researchers
Period of validity:
N/A
Approval date:
March 2022
Date of amendments:
N/A
Year:
2026
Databases:
PubMed, Embase, Web of Science, Cochrane Central Register of Controlled Trials, Scopus, Sinomed
Topic:
Shoulder impingement syndrome
Intervention:
Corticosteroid injection under ultrasound guidance
Study design:
Randomized controlled trials
Number of records identified:
48–86 per database
Search terms:
Disease, Study design, Corticosteroids, Intervention
Language:
English
Document type:
Supplementary material
Year:
Not applicable
Region / City:
Not applicable
Subject:
Research ethics and manuscript submission
Document Type:
Submission Template
Organization / Institution:
Not applicable
Author:
Not applicable
Target Audience:
Researchers, Authors submitting manuscripts
Period of validity:
Not applicable
Approval Date:
Not applicable
Date of Changes:
Not applicable
Note:
Year
Region / City:
Buffalo, NY
Topic:
Research Study Consent
Document Type:
Informed Consent Form
Institution:
University at Buffalo
Author:
University at Buffalo Research Compliance
Target Audience:
Research Participants
Year:
2016
Region / City:
United States
Topic:
Electronic Informed Consent (eIC)
Document Type:
Guidance
Agency / Institution:
Office for Human Research Protection (OHRP), Food and Drug Administration (FDA)
Author:
Office for Human Research Protection (OHRP), FDA
Target Audience:
Researchers, IRBs, Clinical Investigators, and Study Participants
Period of Validity:
Ongoing
Approval Date:
December 2016
Date of Revisions:
Not specified
Year:
2018
Region / City:
United States
Theme:
Cancer prevention, clinical trials
Document Type:
Template
Organ / Institution:
National Cancer Institute (NCI), National Institutes of Health (NIH)
Author:
NCI
Target Audience:
Researchers, clinical trial participants
Period of Validity:
Ongoing
Approval Date:
January 19, 2018
Date of Changes:
N/A
Note:
Year
Topic:
Human Subject Research
Document Type:
Informed Consent Form
Organization / institution:
Coastal Carolina University
Author:
[PI Name]
Target Audience:
Potential research participants
Year:
Not specified
Region / City:
Not specified
Topic:
Research ethics, informed consent
Document Type:
Addendum
Institution / Organization:
Columbia University
Author:
Not specified
Target Audience:
Research participants
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified