№ lp_1_2_38357
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This document outlines the terms and conditions of a clinical trial agreement between a research institution and a clinical research organization (CRO) for the conduct of a study involving pharmaceuticals in Denmark.
Note:
Year
Subject:
Clinical trials, pharmaceutical studies
Document Type:
Agreement
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2015
Region / city:
Canberra
Subject:
Mental Health, Forensic Mental Health, Conditional Release
Document type:
Procedure
Organization / institution:
Canberra Health Services
Author:
Canberra Health Services
Target audience:
CHS staff, especially Mental Health, Justice Health, and Alcohol and Drug Services (MHJHADS) staff
Period of validity:
Ongoing
Approval date:
Not specified
Date of amendments:
Not specified
Year:
2023
Region / City:
N/A
Topic:
Clinical Trials, Sponsor and CRO Engagement
Document Type:
Agenda
Organization / Institution:
N/A
Author:
N/A
Target Audience:
Sponsor and CRO teams
Period of Effect:
N/A
Approval Date:
N/A
Revision Date:
N/A
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:
20
Region / City:
Minnesota
Topic:
Clinical Trials, Research Agreements
Document Type:
Agreement
Organization / Institution:
University of Minnesota
Author:
Not specified
Target Audience:
Sponsors, Contract Research Organizations (CROs), Universities, Clinical Researchers
Duration:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Theme:
Clinical research, communication with sponsor/CRO
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
[INSTITUTION]
Target Audience:
Clinical research personnel, sponsor, CRO
Year:
2026
Region / City:
Barcelona, Spain
Type of Document:
Legal Agreement / Contract
Institution:
Hospital Universitari Vall d’Hebron; Fundació Hospital Universitari Vall d’Hebron - Institut de Recerca
Author / Signatories:
Dr. Albert Salazar i Soler, Dr. Begoña Benito Villabriga, Sponsor representative, CRO representative
Protocol Code:
[•]
EudraCT / EU CT Number:
[•]
Scope:
Clinical trial with medicinal products
Applicable Law:
Spanish national law, EU regulations, GDPR, RD 1090/2015, Regulation (EU) 536/2014, Law 41/2002
Target Audience:
Principal Investigator and research team
Effective Date:
Upon approval by regulatory authority and Ethics Committee
Responsibilities:
Sponsor, CRO, HUVH, VHIR, Principal Investigator
Confidentiality:
Required for all parties regarding trial data and personal data
Regulatory framework:
EASA Part 21
Subject:
Demonstration of design capability through Alternative Procedures to DOA
Document type:
Regulatory manual template
Applicable approvals:
Supplemental Type Certificate, Major Change, Repair Design
Issuing authority:
European Union Aviation Safety Agency
Referenced regulations:
Part 21 Subpart J, AMC 21.A.14(b), GM 21.A.112B
Intended users:
STC applicants and holders
Scope:
Design, certification, and continued airworthiness activities
Language:
English
Structure:
Manual with defined parts, procedures, and appendixes
Status:
Template with placeholder sections
Manual type:
Compliance demonstration documentation
Year:
2026
Region / Country:
United Kingdom
Document Type:
Registration Form
Institution:
Learning Records Service (LRS)
Author:
LRS Administration
Target Audience:
Learning/Training Providers, Subcontractors
Required Identifier:
UK Provider Reference Number (UKPRN)
Submission Method:
Email to LRS Helpdesk
Signatory Requirements:
Director, Secretary, or Headteacher
Related Services:
LRS portal, ULN submission, Individualised Learner Record (ILR)
Year:
2025
Region / City:
England
Theme:
Fisheries, Quota Allocation
Document Type:
Application Form
Organisation:
Marine Management Organisation (MMO), Department for Environment, Food and Rural Affairs (DEFRA)
Author:
Marine Management Organisation (MMO), DEFRA
Target Audience:
Producer organisations, English-registered vessels, and non-sectoral over-10-metre vessels
Period of Action:
2026 quota allocation
Approval Date:
14 October 2025
Modification Date:
Not specified
Note:
Year
Topic:
Clinical Trials
Document Type:
Agreement Template
Organization:
Contract Research Organisation
Target Audience:
Sponsors, CROs, Clinical Trial Sites
Year:
2026
Region / City:
Not specified
Theme:
Compliance Monitoring, Training Organisations
Document Type:
Guidance
Authority / Institution:
Civil Aviation Authority (CAA)
Author:
Not specified
Target Audience:
Small non-complex ATOs offering LAPL, PPL and associated ratings training
Period of Validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2024
Region / City:
European Union
Subject:
EudraVigilance Registration
Document Type:
Registration Form
Authoring Organisation:
European Medicines Agency (EMA)
Target Audience:
Sponsors of clinical trials
Effective Period:
Not specified
Approval Date:
10 December 2024
Modification Date:
Not specified
Note:
Year
Subject:
Data Protection, GDPR Compliance
Document Type:
Agreement, Data Processing Agreement
Target Audience:
Participating NHS / HSC Organisations, Sponsors
Contextual description:
Data processing agreement for non-commercial research studies between Sponsor and Participating NHS / HSC Organisation.
Year:
2022
Region / City:
Kent, Surrey, Sussex
Theme:
Research Development, Health & Social Care
Document Type:
Application Form
Organization:
ARC KSS
Author:
ARC KSS Academy
Target Audience:
Early career researchers, health or social care professionals
Period of validity:
N/A
Approval Date:
2022-04-29, 2022-09-16
Date of Updates:
N/A
Context:
Application form for individuals working in health or social care in Kent, Surrey, and Sussex to apply for the ARC KSS Individual Development Award for applied research.
Year:
2023
Region / City:
Republic of Ireland
Subject:
Clinical Trials
Document Type:
Agreement
Organization / Institution:
Health Service Executive (HSE), Irish Pharmaceutical Healthcare Association (IPHA)
Author:
Not specified
Target Audience:
Sponsors, Contract Research Organisations (CROs), Clinical Organisations
Period of Effect:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Context description:
This document outlines the standard model agreement for clinical trials between sponsors, CROs, and clinical organizations in Ireland.
Year:
2024
Note:
Region / City
Theme:
Research Study Setup
Document Type:
Template
Target Audience:
Sponsor/Co-Sponsors, Participating NHS/HSC Organisations
Issue number:
5
Publication date:
Jun-23
Next major review date:
Jun-28
Document reference:
NS-TAST-GD-061
Record reference number:
2020/127012
Organisation:
Office for Nuclear Regulation
Document type:
Technical assessment guide
Professional lead:
Human and Organisational Capabilities
Author:
Nuclear Safety Inspector
Approved by:
Nuclear Safety Inspector
Subject area:
Nuclear safety, staffing levels, task organisation
Intended audience:
ONR Human Factors Specialist Inspectors
Applicable facilities:
New and existing nuclear facilities
Regulatory context:
Nuclear Site Licence Conditions
Scope:
Staffing arrangements, task organisation, shift patterns, team design
Year:
2011
Region / City:
United Kingdom
Theme:
Charity Law, Legal Structure for Charities
Document Type:
Model Constitution
Organisation:
Charity Commission
Author:
Charity Commission
Target Audience:
Charitable organisations seeking to incorporate as CIO
Period of Validity:
Ongoing
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
2023
Region / City:
Eastern Caribbean
Theme:
Stakeholder engagement, Education, Innovation, Regional Collaboration
Document Type:
Project Plan
Organization / Institution:
Organisation of Eastern Caribbean States (OECS)
Author:
OECS Commission
Target Audience:
Stakeholders involved in post-secondary education and regional innovation
Period of Effectiveness:
Ongoing
Approval Date:
22 August 2023
Date of Changes:
Not specified
Note:
Year
Description:
This document serves as a reference checklist comparing CAAS Maintenance Organisation Exposition and Supplement against SAR-145 requirements.