№ lp_1_2_35776
File format: docx
Character count: 19114
File size: 1792 KB
This is a report evaluating the application for consent to decommission Hunterston B nuclear power station, assessing environmental impacts and public consultation results, recommending granting consent with conditions.
Year:
2024
Region / City:
West Kilbride, Scotland
Topic:
Nuclear Decommissioning
Document Type:
Project Assessment Report
Organ / Institution:
Office for Nuclear Regulation
Author:
EDF Energy Nuclear Generation Ltd
Target Audience:
Public, regulatory bodies, environmental agencies
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
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Year:
2025
Region / City:
Somerset
Subject:
Nuclear Decommissioning, Environmental Impact Assessment
Document Type:
Project Assessment Report
Organization / Institution:
Office for Nuclear Regulation (ONR)
Author:
EDF Energy Nuclear Generation Ltd
Target Audience:
Regulatory bodies, Environmental agencies, Nuclear industry professionals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Revisions:
Not specified
Year:
2025
Region / city:
Hunterston B
Subject:
Nuclear Safety, Decommissioning, Radiological Safety
Document Type:
Safety Case Report
Organization / Institution:
Office for Nuclear Regulation (ONR)
Author:
Project Inspector, Operating Reactors Sub-Directorate, ONR
Target audience:
Regulatory bodies, nuclear safety specialists
Period of validity:
Indefinite, periodic review required
Approval date:
July 25, 2025
Date of revisions:
N/A
Year:
2025
Region / City:
Hunterston B
Topic:
Nuclear Safety, Emergency Response Plan
Document Type:
ONR Project Assessment Report
Organization:
Office for Nuclear Regulation
Author:
Not specified
Target Audience:
Not specified
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2017
Region / City:
Hunterston, North Ayrshire
Subject:
Community funding guidelines
Document Type:
Application form
Organization:
SSE
Target Audience:
Community groups in Cumbrae and Largs
Action Period:
Yearly
Approval Date:
Not specified
Modification Date:
Not specified
Note:
File Number
Region / City:
Delaware, New Castle County, Kent County, Sussex County
Theme:
Guardianship, Consent Affidavit
Document Type:
Legal Affidavit
Authority / Institution:
The Family Court of the State of Delaware
Author:
Affiant
Target Audience:
Parents and guardians involved in custody and guardianship matters
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
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
Year:
2020
Region / City:
United Kingdom
Topic:
Patient consent, publication, medical materials
Document Type:
Consent Form
Organization:
British Association of Dermatologists
Author:
Not specified
Target Audience:
Health professionals, researchers, clinicians
Period of validity:
N/A
Approval Date:
April 2020
Modification Date:
N/A
Context:
Consent form for patients or their representatives to allow the British Association of Dermatologists to use medical materials in publications, ensuring anonymity and outlining the terms of usage.
Year:
2016
Region / City:
Wisconsin
Topic:
Background Check Consent
Document Type:
Form
Organization / Institution:
Wisconsin Department of Administration
Author:
Wisconsin Department of Administration
Target Audience:
Job applicants in Wisconsin
Effective Period:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Topic:
Vaccination Consent
Document Type:
Consent Form
Target Audience:
Patients, Healthcare Providers
Year:
2023
Region / City:
Dublin, Ireland
Topic:
Research Ethics, Consent Forms, Health Research
Document Type:
Consent Form
Author:
Joint SJH / TUH Research Ethics Committee
Target Audience:
Researchers, Study Participants
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Topic:
Informed consent for research participation
Document Type:
Consent Form
Institution:
Saint Francis University
Author:
[Insert name(s) of investigator(s)]
Target Audience:
Research subjects
Year:
2026
Region / City:
Massachusetts
Topic:
Medical License Sanction
Document Type:
Consent Order
Organization / Institution:
Board of Registration in Medicine
Author:
Ellen Hilsinger, M.D., Thomas Bright, Esq., Rachel N. Shute, Esq., Booker T. Bush, M.D.
Target Audience:
Medical Professionals, Legal Counsel, Regulatory Bodies
Effective Period:
Not specified
Approval Date:
13th January 2026
Modification Date:
Not specified
Year:
2023
Region / City:
University of Kentucky
Subject:
Research Study Participation
Document Type:
Consent Form
Institution:
University of Kentucky
Author:
Research Team
Target Audience:
Potential research participants
Study Duration:
Variable (hours, days, months, years)
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Topic:
Research Ethics, Consent Forms
Document Type:
Guidance
Organization / Institution:
UWE Research Ethics Office
Target Audience:
Researchers, Ethics Committees
Year:
2014
Region / City:
United States
Subject:
Research ethics, IRB review process
Document type:
Checklist
Author:
Not specified
Target audience:
IRB members, Designated Reviewer, researchers
Period of validity:
Ongoing
Approval date:
3/25/14
Amendment date:
11/1/2024
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