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Kliniske studier (NorCRIN)
Checklists and Templates
Database Lock Form - Template
Checklists and Templates
Protocol - Template
Protocol Content Checklist - Template
Protocol Synopsis - Template
Data Monitoring Committee Charter - Template
Clinical Trial Protocol Site Signature Form - Template
Statistical Analysis Plan - Template
Feasibility Questionnaire - Template
Safety Reporting Specifics - Template
Data Processing agreement SUSAR reporting - Template
DSUR - Template
Individual Case Report Form Eudravigilance - Template
Checklist Initiation of Clinical Trial - Sponsor - Template
Checklist Conduct of Clinical Trial - Centre - Template
Checklist Conduct of Clinical Trial - Sponsor - Template
Checklist Completion of Clinical Trial - Centre - Template
Checklist Completion of Clinical Trial - Sponsor - Template
Trial Master File (TMF) Table of Content Muliticenter Trial - Template
TMF Index Divider Multicenter Trial - Template
Investigator’s Site File (ISF) Table of Content - Template
ISF Index Divider - Template
TMF/ISF Table of Content Single Center Trial - Template
TMF/ISF Index Divider Single Center Trial - Template
Location of Document if not in ISF - Template
Informed Consent Form Version Tracking Log - Template
Protocol Version Tracking Log - Template
Contact Information Study Team - Template
Meeting Participants List - Template
Delegation Log - Template
Signature Log - Template
Prescreening Log - Template
Screening Log - Template
Identification & Enrollment Log - Template
Laboratory Sample Storage Log - Template
Source Data List - Template
Pharmacy File Table of Contents - Template
Archiving log - Template
Labels for Archiving - Template
Training Log - Template
Investigator's Brochure Checklist - Template
Investigator's Brochure (IB) - Template
IMP Requisition Form - Template
IMP Temperature Log - Template
IMP Accountability Form with Kit or ID-Number - Template
IMP Accountability Form Common Stock Unnumbered - Template
IMP Accountability Form Different Manufacturers - Template
IMP Reconciliation - Template
IMP Destruction - Template
IMP Handling Checklist - Template
Start-up Meeting Agenda - Template
Start-up Meeting Checklist - Template
Compliance Norwegian Requirements on Data Protection - Template
Financial and Other Arrangements - Template
Description first SM after transition - Template
Vurdering av monitoreringsbehov kliniske studier - Templat
Risk assessment site checklist prior to start - Template
Risk Assessment Plan - Template
Principal Investigator (PI) Site Risk Evaluation Checklist Prior to Study Initiation - Template
Monitoring Plan - Template
Protocol Deviation Handling Plan - Template
Protocol Deviation Notification and Tracking Form - Template
Protocol Deviation Log Single Center Study - Template
Protocol Deviation Log Multicenter Study - Template
Data Management Plan - Template
Data Management Report - Template
Data Management Personnel Log - Template
User Acceptance Testing (UAT) - Template
DEA Approval Form - Template
DEA Change Log - Template
Database Lock Form - Template
Database Unlock Form - Template
Database Relock Form - Template
Privacy Notice for Clinical Trial Staff - Template
CV for Investigators - Template
CV for Non-investigators - Template
Agreement Multicentre Trial - Template
Agreement for Support from External/Commercial Source - Template
Agreement for Transfer of Clinical Trial Tasks in Decentralised Trials - Template
Power of Attorney - Template
Økonomisk avtale apotek - Template
Samarbeidsavtale apotek - Template
Avtale med forskningsstøtte - Template
Tilleggsavtale med forskningsstøtte - Template
Trial Initiation Report - Template
Monitoring Report - Template
Close-out Monitoring Report - Template
Biobank Monitoring Report - Template
Trial Handover Procedure and Checklist - Template
Query List - Template
Green Light for Trial Site - Template
Data Processing Agreement for Monitoring Services - Template
Data Verification Plan - Template
Co-monitoring Visit Report - Template
Database Lock Form - Template
Sist oppdatert: 08.03.2025
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Utgiver: NorCRIN
Versjon: 1.0
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