№ lp_1_21524
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These documents comprise various safety and environmental management procedures, policies, and guidelines issued by the National Energy Technology Laboratory (NETL), detailing protocols for safety, health, environmental standards, and regulatory compliance.
Year:
2011
Region / City:
Not specified
Subject:
Safety, Health, Environmental Management
Document Type:
Manuals, Procedures, Directives
Organization:
National Energy Technology Laboratory (NETL)
Author:
Not specified
Target Audience:
Employees, Safety and Health Personnel
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2016
Region / City:
United States
Topic:
Energy Technology, Fossil Energy
Document Type:
Overview
Organization:
National Energy Technology Laboratory (NETL)
Author:
National Energy Technology Laboratory (NETL)
Target Audience:
Policymakers, Researchers, Energy Sector Professionals
Period of Activity:
2016 and ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2023
Region / City:
NETL
Topic:
Citrix Access and Login Instructions
Document Type:
User Guide
Organization / Institution:
NETL
Author:
NETL IT Department
Target Audience:
NETL employees and contractors
Effective Period:
Ongoing
Approval Date:
September 2023
Modification Date:
September 2023
Department:
U.S. Department of Energy/National Energy Technology Laboratory (NETL)
Duty Location:
Albany, OR
Academic Level:
PhD
Position Type:
Postdoctoral Research Appointment
Appointment Duration:
1 year
Work Schedule:
Full time (40 hours per week)
Possibility of Extension:
Yes
Closing Date:
6/30/2018
Eligibility:
United States Citizens, LPRs, and approved Foreign Nationals including F-1 OPT with EAD (STEM extension not valid), J-1 Exchange Visitor, and LPR with EAD
Research Focus:
Computational modeling of thermo-chemo-mechanical behavior of structural alloys in extreme environments
Primary Methods:
Phase-field modeling, finite element method, high-performance computing (MPI, parallel processing)
Application Process:
Online application through ORISE program and CV submission by email
Contact Person:
Youhai Wen
Administrative Contact:
Patricia Adkins-Coliane, NETL Graduate Education Program Manager
Year:
2019
Region / City:
Germantown, MD; College Park, MD; Washington, DC; Chantilly, VA
Subject:
Classification Support Services
Document Type:
Request for Proposal (RFP)
Agency / Institution:
U.S. Department of Energy, National Energy Technology Laboratory
Author:
Office of Classification within EHSS
Target Audience:
Small business contractors
NAICS Code:
541690
Business Size Standard:
$15 million
Contract Type:
Firm-fixed-price and cost-plus-award-fee CLINs
Performance Period:
1 year base with four 1-year options
Submission Deadline:
April 19, 2019, 4:00 PM Eastern Local Time
Question Deadline:
April 9, 2019
Locations of Work:
DOE Germantown facility, NARA College Park, Forrestal Building Washington, DC, CIA Chantilly facility
Travel Requirements:
Local, domestic, and/or international
Year:
2015
Region / City:
Saudi Arabia
Topic:
Medical Education
Document Type:
Framework
Institution:
Ministry of Higher Education
Target Audience:
Medical educators, policymakers, academic institutions
Period of Validity:
2012-2015
Approval Date:
January 2015
Date of Last Changes:
N/A
Year:
2020
Region / city:
UNESCO Headquarters, Paris
Subject:
Revision of Operational Directives for the implementation of the Convention
Document type:
Official Report
Institution:
UNESCO
Author:
Intergovernmental Committee
Target audience:
States Parties to the Convention
Period of validity:
2020-2021
Approval date:
2020-09-10
Date of changes:
2020
Context:
Official record of the eighth session of the General Assembly discussing revisions to the Operational Directives regarding the nomination and evaluation process under the Convention for Safeguarding Intangible Cultural Heritage.
Year:
2023
Region / City:
United States
Topic:
Sustainability, Certification, Soybean Production
Document Type:
Protocol
Organization / Institution:
Soy Export Sustainability, LLC (SES)
Author:
Soy Export Sustainability, LLC (SES)
Target Audience:
SSAP/RED system users, Certification Bodies, EU Member States
Period of Validity:
Not specified
Approval Date:
November 2023
Date of Changes:
Version 2.3
Year:
2016
Region / City:
Dartford, Kent
Subject:
Compliance Declaration for Refrigeration and Heat Pump Systems
Document Type:
Declaration of Compliance
Organ / Institution:
J & E Hall International
Note:
Author
Target Audience:
Industry professionals, regulatory bodies
Year:
2016
Region / City:
California
Subject:
Strategic Directives, Governance Process, Commission Policies
Document Type:
Commission Policy
Author:
California Public Utilities Commission
Target Audience:
Stakeholders, regulatory bodies, utility companies, consumers
Period of Validity:
Ongoing
Approval Date:
June 23, 2016
Revision Date:
N/A
Year:
2020
Region / City:
North West
Theme:
Court Access Management
Document Type:
Directive
Author:
Ms JJ Ikaneng, Chief Magistrate
Target Audience:
District Court Staff, Legal Professionals, Law Enforcement
Action Period:
27/03/2020 to 16/04/2020
Approval Date:
23/03/2020
Date of Amendments:
None
Note:
Context
Year:
20__
Region / City:
Miami-Dade County, Florida
Theme:
Guardianship
Document Type:
Court Order
Organization / Institution:
Circuit Court of the Eleventh Judicial Circuit
Author:
Circuit Judge
Target Audience:
Legal professionals, Guardians, Court officials
Period of validity:
Until further court order
Date of approval:
_, 20
Date of amendments:
Not specified
Year:
2019
Location:
Hawai‘i Pacific Health, Learning Resource Center, Room 101, 793 S Hotel Street (Next to Straub Medical Center)
Topic:
Advance Care Planning, Advance Directives, POLST
Document Type:
Training Course
Organization:
Hawai‘i Pacific Health
Author:
Hawai‘i Pacific Health ACP Coordinator, Michelle Cantillo
Target Audience:
Nurses, Physicians, Social Workers, Clinicians
Event Dates:
February 26, 2019; May 14, 2019; August 21, 2019; December 11, 2019
Approval Date:
N/A
Change Date:
N/A
Year:
2009–2017
Location:
Oregon, USA
Topic:
Advance directives and end-of-life care
Document type:
Case study
Institution:
Local court, nursing facility
Subjects:
Bill Harris, Nora Harris
Medical condition:
Alzheimer’s disease, dementia
Legal context:
State laws on elder abuse, court rulings on feeding refusal
Ethical considerations:
Patient autonomy, right-to-die, end-of-life decision-making
Previous interventions:
Hospice enrollment, medical feeding management
Family involvement:
Spouse and children affirming advance directive
Year:
2022
Region / Country:
Scotland, United Kingdom
Subject:
Food safety regulation; animal feed; food contact materials; extraction solvents; legislative alignment after EU exit
Document type:
Consultation response summary report
Institution:
Food Standards Scotland
Publication date:
23 November 2022
Consultation period:
12 September 2022 – 10 October 2022
Legal context:
Amendments to domestic legislation following the United Kingdom’s withdrawal from the European Union
Related legislation:
Directive 2009/32/EC
Respondent organization:
UK Flavour Association
Number of responses received:
1
Geographical scope:
Scotland
Audience:
Government ministers, regulatory authorities, food industry stakeholders
Year:
2023
Region / Country:
United States
Topic:
Advance Directives and End-of-Life Decisions
Document Type:
Educational/Informational Material
Institution:
University of North Carolina Health Care / American Bar Association
Authors:
Various (cited sources include Dowbiggin I., DIRECTIVES A., Santonocito C. et al.)
Target Audience:
Healthcare professionals, occupational therapists, patients
Legal References:
Patient Self-Determination Act (1991), state-specific advance directive laws
Key Cases:
Cruzan v. Director, Missouri Department of Health; sample case from North Carolina
Document Sections:
Types of advance directives, Living Will, Health Care Power of Attorney, Legal Guardianship, POLST, DNR
Resources:
US Living Will Registry, ABA myths and facts on advance directives, literature review on advance directives
Year:
2024
Month:
March
Document Code:
CL:O-AWS034
Subject:
Mandatory Continuing Airworthiness Information (MCAI) Compliance
Topic:
Airworthiness Directives and Service Bulletins Oversight
Document Type:
Inspection Checklist and Record Form
Organization:
Civil Aviation Safety and Security Oversight Agency
Sector:
Civil Aviation Safety
Purpose:
Evaluation of operator compliance with Airworthiness Directives and Service Bulletins
Key Sections:
Inspection Record; General Assessment; Inspectors Remarks; Recommendation; Manager FSS Remarks
Assessment Codes:
YES = Satisfactory; NO = Not Satisfactory; N/C = Not Checked; N/A = Not Applicable
Fields for Operator Information:
Name of Operator; Physical Address (Location); Postal Address
Aircraft Information:
Type/Series of Aircraft
Evaluation Information:
Date of Evaluation; Inspectors
Compliance Areas:
Procedures for receiving ADs/SBs; implementation of Airworthiness Directives; maintenance certification; inspection procedures; defect reporting; maintenance manual conformity
Approval Section:
Inspector Signature and Date; Manager FSS Approval Signature and Date
Year:
2020
Region / City:
North West Administrative Region, Mmabatho
Subject:
Court access and case management during COVID-19 lockdown
Document Type:
Official directive
Institution:
Office of the Chief Magistrate
Author:
Ms JJ Ikaneng, Chief Magistrate
Target Audience:
District court staff, legal practitioners, law enforcement
Effective Period:
27 March 2020 – 16 April 2020
Date Issued:
23 March 2020
Legal Basis:
Section 8(3) of the Superior Courts Act, 2013
Contact:
0836511055
Year:
2023
Region / City:
Texas
Topic:
Healthcare, Patient Safety, Advance Directives
Document Type:
Report
Organization / Institution:
Houston Methodist
Author:
Pat Harrison
Target Audience:
Public, Legislators, DMV, Healthcare Providers
Duration:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.