№ files_lp_4_process_2_45674
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Character count: 13318
File size: 52 KB
Provides procedural guidance for monitoring, documenting, and reporting medical events for participants in neuromodulation research studies at KSCIRC, including roles and responsibilities of all research personnel.
Year:
2026
Organization:
Kennedy Space Center International Research Center (KSCIRC)
Document Type:
Standard Operating Procedure
Audience:
Research staff, investigators, clinicians, and medical monitors
Scope:
Oversight of research participants with spinal cord injuries
Authors:
Principal Investigator and study team
Medical Oversight:
Study Physician, Research Nurse, Co-Investigator, Participating Clinician
Monitoring Period:
Throughout participant involvement in study
Reporting Requirements:
Adverse events and weekly progress updates
Related Appendices:
Medical Clinical Oversight, Research Medical Log, Weekly Update, Adverse Event Report Form
Price: 8 / 10 USD
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Year:
Not specified
Region / City:
Not specified
Topic:
Research funding, neurofeedback, neuromodulation
Document Type:
Grant Application
Organization / Institution:
Bio-Medical Instruments (BMI), Foundation for Neurofeedback and Neuromodulation Research
Author:
Not specified
Target Audience:
Full-time students in healthcare/mental health care academic programs
Validity Period:
12 months from receipt of funding
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2008
Region / City:
Not specified
Subject:
Neuroscience, Physiology
Document Type:
Student Laboratory Exercise
Institution:
Not specified
Author:
Not specified
Target Audience:
Students, Researchers in Neuroscience
Period of Activity:
Not specified
Date of Approval:
Not specified
Date of Changes:
Not specified
Contextual Description:
Laboratory exercises for understanding synaptic transmission and neuromodulation through crayfish models, aimed at students studying neuronal physiology.
Year:
2019
Region / city:
OECD
Topic:
Adverse Outcome Pathway, oxidative stress, brain development, neurotoxicity
Document Type:
External Review Report
Author:
OECD EAGMST review manager
Target Audience:
Scientific community, regulators, policymakers
Period of validity:
Not specified
Approval Date:
June 2018
Date of revisions:
17 March 2020
Year:
2024
Region / city:
UK
Topic:
Climate change, extreme weather, workplace safety
Document type:
Policy document
Organization / institution:
UNISON, TUC
Author:
UNISON
Target audience:
Trade union representatives, employers, workers
Period of validity:
2024–2025
Approval date:
Not specified
Date of changes:
Not specified
Note:
Year
Year:
2003
Region / City:
Mount Sinai Hospital
Subject:
Clinical Research
Document Type:
Guideline
Organization / Institution:
Mount Sinai Hospital REB
Author:
REB Chair
Target Audience:
Clinical Investigators, Research Staff
Effective Period:
Ongoing
Approval Date:
November 6, 2003
Revision Date:
July 8, 2015
Year:
2026
Region / City:
Boston, MA
Topic:
Clinical Research, Adverse Event Reporting
Document Type:
Form
Author:
BU Medical Campus
Target Audience:
Clinical research staff
Period of validity:
Ongoing
Approval Date:
2026-01-01
Date of Changes:
Not specified
Year:
2019
Region / City:
International
Subject:
Medical device adverse event reporting
Document Type:
Proposed document
Organ / Institution:
International Medical Device Regulators Forum (IMDRF)
Author:
IMDRF Adverse Event Terminology Working Group
Intended Audience:
Regulatory authorities, healthcare providers, manufacturers, reporters of adverse events
Period of validity:
Not specified
Approval date:
27th June 2019
Date of Changes:
Not specified
Year:
Not specified
Region / City:
Not specified
Topic:
Adverse events tracking in clinical studies
Document Type:
Template
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Site Monitors, Principal Investigators, study team members
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Modifications:
Not specified
Year:
2020
Region / City:
International
Topic:
Medical device regulation
Document Type:
Final Document
Organization / Institution:
International Medical Device Regulators Forum (IMDRF)
Author:
IMDRF Adverse Event Terminology Working Group
Intended Audience:
Regulatory authorities, medical device manufacturers, healthcare providers
Period of Validity:
Not specified
Approval Date:
18 March 2020
Date of Changes:
Not specified
Note:
Year
Theme:
Healthcare, Medication Safety, Adverse Drug Event Prevention
Document Type:
Program Evaluation Report
Organization / Institution:
Centers for Medicare & Medicaid Services (CMS)
Target Audience:
Healthcare Providers, Medicare Beneficiaries, Policymakers
Year:
2022
Region / City:
N/A
Topic:
Adverse Reaction Tracking, Drug Allergy Management
Document Type:
User Manual
Institution:
Department of Veterans Affairs
Author:
N/A
Target Audience:
Healthcare professionals in the Veterans Health Administration
Period of Validity:
N/A
Approval Date:
September 2022
Date of Amendments:
N/A
Year:
2025
Region / City:
United States
Subject:
Serious Adverse Event Reporting
Document Type:
Form
Organization / Institution:
National Cancer Institute (NCI)
Author:
National Cancer Institute
Target Audience:
Clinical Investigators, Medical Monitors, Research Staff
Effective Period:
Ongoing
Approval Date:
09/04/2025
Modification Date:
10/01/2024
Note:
Year
Subject:
Health Insurance Appeals
Document Type:
Notification
Target Audience:
Insurance claimants
Year:
2023/2024
Region/City:
Capital, Coast and Hutt Valley
Theme:
Healthcare, Patient Safety
Document Type:
Report
Organization/Institution:
Health New Zealand | Te Whatu Ora
Author:
Health New Zealand | Te Whatu Ora
Target Audience:
Healthcare professionals, policymakers, public health officials
Period of Validity:
1 July 2023 – 30 June 2024
Approval Date:
September 2025
Date of Changes:
Not specified
Year:
2024
Region / city:
Australia
Topic:
Adverse Childhood Experiences, Trauma, Mental Health
Document type:
Factsheet
Organization / institution:
New South Wales Department of Education
Author:
Unknown
Target audience:
Educators, Researchers, Policymakers
Period of validity:
Not specified
Date of approval:
Not specified
Date of changes:
Not specified
Year:
2023
Region / City:
N/A
Topic:
Registration Service, Operational Choreography
Document Type:
Change Request
Organization:
MHHS Programme
Author:
N/A
Target Audience:
Programme Participants
Period of Validity:
N/A
Approval Date:
08/02/2023
Date of Changes:
N/A
Organization:
United Nations Development Programme
Country:
Kuwait
Document type:
Standard Operating Procedures
Subject area:
Project cycle management
Implementation modality:
National Implementation Modality with Country Office support
Strategic framework:
UNDP Strategic Plan 2014–2017
Programme framework:
Country Programme Document and Country Programme Action Plan 2015–2018
Responsible institution:
UNDP Kuwait Country Office
Government coordinating agency:
General Secretariat of the Supreme Council for Planning and Development
Scope:
UNDP programmes and projects implemented in Kuwait
Project phases covered:
Formulation, appraisal, implementation, monitoring, evaluation, extension and closure
Intended users:
UNDP staff and national implementing partners
Annexes included:
Capacity assessment checklist, project document template, risk logs template, quality assurance checklist
Year:
Contract Year No.
Supplier:
Legal Name of Supplier
Facility:
Name of Facility
Contract:
Contract Title / Contract ID
Contract Date:
Contract Date
Time Period:
From insert date To insert date
Contract Capacity (MW):
Contract Capacity
Planned Outages:
As specified per unit and month
Unplanned Outages:
Percentage per unit and month
Overall Availability:
Percentage per unit and month
Type of Document:
Prescribed Form – Annual Operating Plan
Audience:
Buyer and Contract Management
Source:
Independent submission under Section 14.3(b)(i) of the Contract