№ lp_1_2_65471
File format: docx
Character count: 84501
File size: 156 KB
This document outlines a comprehensive guide for clinical practice in Interventional Radiology, covering various diagnostic and interventional procedures, patient preparation, and post-procedure management in a medical setting.
Year:
Spring 2009
Region / City:
Dartmouth-Hitchcock Medical Center
Subject:
Interventional Radiology Procedures
Document Type:
Clinical Manual
Institution:
Dartmouth-Hitchcock Medical Center
Author:
Not specified
Target Audience:
Medical professionals in interventional radiology
Effective Period:
Ongoing for clinical rotations
Approval Date:
Spring 2009
Date of Last Revision:
Not specified
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:
2018
Region / city:
Vale of York, Scarborough and Ryedale
Theme:
Varicose Veins Management
Document type:
Commissioning Policy
Organization:
NHS Vale of York and Scarborough and Ryedale CCGs
Author:
Not specified
Target audience:
Healthcare professionals, Primary care clinicians, Vascular surgeons
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
2018
Document type:
Guidance document
Subject:
Informed consent in interventional clinical trials
Population:
Healthy adult participants
Scope:
Interventional clinical trials with trial medicine
Jurisdiction:
Belgium
Organizations mentioned:
CT College; Healixia; Ethics Committees; Belgian Data Protection Authority
Language versions:
English; French; Dutch
Intended users:
Clinical trial sponsors
Regulatory context:
Ethics Committee submission requirements
Version:
1.0
Year:
2024
Region / City:
Ireland
Topic:
Clinical Trials, Legal Agreements, Healthcare
Document Type:
Explanatory Note
Organization:
HSE, IPHA
Target Audience:
Contract Research Organizations, Hospitals, Pharmaceutical Companies
Effective Date:
20.05.24
Related Date:
20.05.24
Approval Date:
20.05.24
Year:
2021
Region / City:
Brussels
Topic:
Clinical Research Ethics
Document Type:
Submission Form
Institution:
Saint-Luc University Clinics (CUSL)
Author:
Ethics Committee
Target Audience:
Researchers, Clinical Trial Investigators
Period of Validity:
2021-2022
Approval Date:
N/A
Date of Changes:
N/A
Year:
2019
Region / City:
Toronto, Canada
Topic:
Informed consent, Clinical trial
Document Type:
Template, Informed consent form
Institution:
SickKids
Author:
SickKids REB
Target Audience:
Parents, Researchers
Effective Period:
N/A
Approval Date:
November 14, 2019
Modification Date:
N/A
Year:
2019
Region / City:
SickKids, Canada
Topic:
Clinical Trial Consent Form
Document Type:
Template
Organization:
SickKids Research Ethics Board
Author:
SickKids
Target Audience:
Research Teams, Clinical Trial Participants
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2024
Region / City:
United Kingdom
Topic:
Health Technology Evaluation
Document Type:
Meeting Minutes
Organ / Institution:
National Institute for Health and Care Excellence (NICE)
Author:
Committee members and NICE staff
Target Audience:
Healthcare professionals, policy makers, and stakeholders in health technology evaluation
Period of validity:
10 October 2024
Approval Date:
10 October 2024
Date of Changes:
None
Note:
Year
Topic:
Clinical Research / Protocol Development
Document Type:
Protocol Template
Organization / Institution:
DMID
Author:
DMID
Target Audience:
Clinical Researchers, Investigators
Year:
2023
Region / city:
Livingstone, Zambia; Lusaka, Zambia; Twickenham, London, UK; Nashville, TN, USA
Subject:
Hypertension, dietary salt, inflammation
Document type:
Research study
Organization / institution:
Mulungushi University, University of Zambia, St. Mary’s University, Vanderbilt University Medical Center
Author:
Sepiso K. Masenga, Leta Pilic, Benson M. Hamooya, Selestine Nzala, Geoffrey Kwenda, Douglas C. Heimburger, Wilbroad Mutale, John R. Koethe, Annet Kirabo, Sody M. Munsaka
Target audience:
Researchers, healthcare professionals
Period of validity:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Document type:
Sponsor statement template
Subject:
Use of Belgian Model Informed Consent Form for vaccine trials in adult healthy volunteers
Related procedure:
Clinical trial application
Scope:
Interventional trials with investigational vaccines
Geographical reference:
Belgium
Applicable to:
Sponsors of clinical trials
Referenced document:
Belgian Model ICF for Vaccine Trials in Adult Healthy Volunteers
Required information:
EU number, trial number, sponsor details, adaptations to mandatory text if applicable
Signature requirement:
Sponsor representative in the Member State
Date format:
DD/MMM/YYYY
Year:
2019
Location:
Minneapolis, MN, USA
Subject:
Construction and Site Preparation for Interventional Radiology Rooms
Document Type:
Government Solicitation / Contract Offer
Issuing Agency:
Department of Veterans Affairs, Program Contracting Activity Central
Author/Contracting Officer:
Bailey E. Donato
Target Audience:
Service-Disabled Veteran-Owned Small Businesses (SDVOSB)
Contract Value:
Between $2,000,000 and $5,000,000
Performance Period:
To be specified in the contract after award
Submission Deadline:
April 16, 2019, 3:00 PM EST
Contract Method:
Sealed Bid / Negotiated RFP
Legal Reference:
38 U.S.C. § 8127 (Public Law 109-461)
Required Documentation:
Performance and payment bonds if applicable, completed offer forms, acknowledgment of amendments
Year:
2018
Region / City:
Minneapolis, MN
Subject:
Interventional Radiology Physician Services
Document Type:
Contract Award Notice
Agency:
Department of Veterans Affairs
Contracting Office:
NETWORK 23 CONTRACTING OFFICE, 316 Robert Street N., St. Paul, MN 55101
Award Number:
36C26318C0043
Award Amount:
$1,497,228.00
Award Date:
02-05-2018
Awardee Name:
MINNEAPOLIS RADIOLOGY
Awardee DUNS Number:
078882836
Awardee Address:
2955 XENIUM LN N STE 40, MINNEAPOLIS, MN 55441
Point of Contact:
[email protected]
NAICS Code:
621111
Set-Aside:
Not specified
Archive Days:
Not specified
Recovery Act Funds:
Not specified
Document Type:
Clinical research record log
Purpose:
Recording protocol deviations occurring at a study site during clinical research studies
Field:
Clinical Research
Research Type:
Observational and Interventional Studies
Maintained In:
Study Binder (Investigator Binder, Regulatory Binder, Investigator Site File, Study File)
Responsible Personnel:
Study coordinators, principal investigators (PIs), site staff
Oversight Bodies:
Institutional Review Board (IRB), Study Sponsor Monitor
Related Procedure:
OHRE/IRB SOP 1401
Deviation Categories:
Informed Consent, Eligibility, Protocol Implementation, Reporting, Other
Deviation Codes:
Standardized numerical codes for protocol deviation classification
Record Structure:
Page-numbered log with reverse chronological storage
Reporting Requirement:
Deviations reported to the IRB according to IRB Standard Operating Procedures
Key Data Fields:
Reference Number, Subject ID, Date of Deviation, Date Identified, Deviation Description, Deviation Type, Adverse Event Indicator, Study Continuation Status, IRB Reporting Requirement, IRB Reporting Date
Year:
[Date]
Type of document:
Quality assurance and audit programme
Institution:
[Name of Dental Practice]
Scope:
Radiology services
Intended audience:
Dental practice staff involved in radiography
Review period:
Annual or as specified
Content:
QA processes, equipment checks, staff training, document control, local rules, radiation risk assessment
Year:
2012
Region / City:
United Kingdom
Topic:
Radiology, Patient Safety, Invasive Procedures
Document Type:
Checklist, Audit
Organization / Institution:
The Royal College of Radiologists, National Patient Safety Agency
Author:
Edward Johnston, P Malcolm
Target Audience:
Radiologists, Radiographers, Nurses, Healthcare Assistants, Radiology Department Assistants
Period of Validity:
N/A
Approval Date:
Monday 21 May 2012
Last Reviewed:
Wednesday 26 June 2019
Context:
A checklist designed to ensure safety compliance for invasive radiological procedures, specifically focusing on peri-procedural safety checks and audit compliance.
Year:
2024
Region / city:
Wellington, New Zealand
Topic:
Pathology and radiology messaging
Document type:
Standard
Organization / institution:
Health New Zealand | Te Whatu Ora
Author:
Health New Zealand | Te Whatu Ora
Target audience:
Health authorities, health service providers, pathology providers, radiology providers, health institutions, health IT vendors, health IT consultants, and the health informatics community
Period of validity:
From September 2024
Approval date:
September 2024
Amendment date:
September 2024
Year:
2026
Region / city:
United Kingdom
Subject:
Medicine / Radiology
Document Type:
Eligibility Criteria
Institution:
General Medical Council (GMC)
Note:
Author
Target audience:
Medical professionals applying for ST1 position in Radiology
Period of validity:
From advertised post start date
Context description:
Detailed eligibility and selection criteria for applying to the ST1 Radiology position in the UK, outlining required qualifications, experience, and competencies.