№ lp_1_2_47772
File format: docx
Character count: 7609
File size: 67 KB
This glossary provides definitions and explanations of terms and acronyms related to clinical trials, offering a comprehensive resource for professionals in the field of clinical research.
Note:
Year
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:
2025
Region / City:
New South Wales
Topic:
Visual Arts, Space Art, Education
Document Type:
Glossary
Organization / Institution:
Department of Education, New South Wales
Author:
State of New South Wales
Target Audience:
Students, Educators
Period of Validity:
2025
Approval Date:
2025
Date of Changes:
N/A
Year:
2022
Region / City:
UK
Theme:
Violence Against Women, Domestic Abuse, Sexual Violence, Safeguarding
Document Type:
Glossary
Author:
Not specified
Target Audience:
Practitioners in the VAWDASV and Safeguarding Sector
Period of Validity:
Not specified
Date of Approval:
Not specified
Date of Changes:
Not specified
Note:
Year
Date:
09/07/2010
Policy Group Acronym:
SPG
Policy Group Name:
Security Policy Group
Document Status:
STATUS
Contact Person:
David Kelsey/STFC, UK
Approved By:
Body who approved the doc
Approved Date:
09/07/2010
Copyright:
Copyright © Members of the EGI-InSPIRE Collaboration, 2010
Note:
Document Log
Issue 1.0:
7 July 2010
Author:
David Kelsey/STFC
Year:
2010
Region / City:
Europe
Topic:
Security Policy
Document Type:
Glossary
Organization:
EGI-InSPIRE
Target Audience:
Researchers, Grid users
Period of Validity:
2010–2014
Approval Date:
09/07/2010
Modification Date:
Not provided
Year:
2023
Region / City:
United States
Topic:
Clinical Trials, Research, Medical Studies
Document Type:
Glossary
Organization / Institution:
National Institutes of Health (NIH)
Author:
National Library of Medicine (NLM)
Target Audience:
Clinical researchers, healthcare professionals, medical librarians
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2025
Region / City:
Not specified
Category:
Glossary
Subject:
Business Continuity, Disaster Recovery, Crisis Management, Risk Management, Emergency Management, Pandemic
Document Type:
Glossary
Organization:
DRJ EAB Glossary Committee
Author:
Volunteers of the DRJ EAB Glossary Committee
Target Audience:
Professionals in business continuity, disaster recovery, and crisis management
Period of Validity:
Indefinite
Date of Approval:
Not specified
Revision Date:
August 2025
Year:
2023
Region / City:
Arkansas
Theme:
Health, Social Services, Medicaid, Healthcare Providers
Document Type:
Glossary
Organization:
Arkansas Department of Human Services
Author:
Not specified
Target Audience:
Healthcare professionals, Social workers, Medicaid providers
Period of validity:
Not specified
Approval Date:
Not specified
Date of amendments:
Not specified
Document type:
Glossary
Jurisdiction:
Nunavut, Canada
Subject:
Surface and subsurface land and resource rights
Issuing body:
Nunavut Surface Rights Tribunal
Legal framework:
Nunavut Land Claims Agreement (1993); Nunavut Waters and Nunavut Surface Rights Tribunal Act (S.C. 2002, c.10)
Author:
T. Bert Rose
Role of author:
Chairperson
Intended users:
Parties involved in surface and subsurface land and resource matters
Geographic scope:
Nunavut
Document status:
Living document
Contact address:
208 Sinna Street, Iqaluit, Nunavut, X0A 2H0
Contact email:
[email protected]
Year:
2000
Region / City:
United States
Subject:
Contract Management, Acquisition, Defense
Document Type:
Glossary
Agency / Institution:
Defense Contract Management Agency (DCMA)
Author:
Not specified
Target Audience:
Functional specialists in DCMA
Period of Action:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Note:
Year
Year:
2023
Region / City:
Noordwijk, The Netherlands
Subject:
Space Systems Terminology
Document Type:
Glossary
Organization:
European Space Agency (ESA)
Author:
ECSS Glossary Task Force
Target Audience:
Space industry professionals, ESA personnel
Period of Validity:
Ongoing
Approval Date:
October 2023
Revision Date:
October 2023
Year:
2023
Category:
Glossary
Source:
DRJ, BCI
Revision Date:
September 2023
Contextual description:
A glossary providing definitions and explanations for various terms related to business continuity, disaster recovery, and emergency management.
Year:
2026
Region / City:
United States
Topic:
Election Processes, Voting Systems
Document Type:
Glossary
Organ / Institution:
Election Assistance Commission (EAC)
Author:
Election Assistance Commission
Target Audience:
Election officials, policymakers, and voting systems professionals
Period of validity:
Ongoing
Approval Date:
N/A
Date of Changes:
N/A
Year:
2024
Region / City:
Pretoria
Subject:
Court Schedules
Document Type:
Court Listing
Institution:
Gauteng Division, Pretoria
Target Audience:
Legal professionals, Court staff
Period of Validity:
20 February 2024
Approval Date:
20 February 2024
Date of Changes:
N/A
Jurisdiction:
Australia
Regulatory framework:
Therapeutic Goods Administration (TGA) Clinical Trial Notification scheme
Document type:
Regulatory notification form
Scope:
Clinical trials involving medicines, biologicals, medical and therapeutic devices
Trial phases covered:
Phase I–IV, bioavailability/bioequivalence, device studies
Subjects:
Human participants
Ethics oversight:
Human Research Ethics Committee (HREC)
Approving authority:
Relevant institutional authority
Geographic coverage:
Australian trial sites with optional international sites
Responsible party:
Lead Investigator
Fee responsibility:
Lead Investigator
Related institution:
La Trobe University
Submission requirement:
Completed form and ethics approval
Note:
Year
Subject:
Clinical Trials, Medical Research
Document Type:
Template
Organization / Institution:
EU Clinical Trials Expert Group
Target Audience:
Sponsors of clinical trials
Document type:
Instructional guidance
Subject:
Informed consent forms in clinical research
Context:
Clinical trials involving human participants
Regulatory and ethical framework:
Research ethics and regulatory compliance
Organizations referenced:
Children’s Oncology Group; National Cancer Institute; National Institutes of Health; OCREB
Funding context:
Public funding by the National Cancer Institute
Intended audience:
Consent form authors; clinical trial investigators; participating centres
Geographic scope:
North America
Population referenced:
Children and adolescents with cancer; parents or legal guardians
Related materials:
Provincial informed consent form templates; lay terminology glossary
Year:
2025
Region / city:
Ireland
Topic:
Clinical trials, Primary care, Research funding
Document type:
Request Form
Organization / institution:
Health Research Board
Author:
HRB Primary Care Clinical Trials Network
Target audience:
Lead Investigators in clinical trials
Effective period:
Until November 2026
Approval date:
N/A
Date of amendments:
N/A