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01 响木最新众筹课
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4000-4999
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4100-4199
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4156.临床试验SOPs(全英文版)
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相关资料
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Attachment - Annual Progress Report Form for CTIMPS.docx
Attachment - Archiving Process Map.docx
Attachment - CI Site Initiation Visit Checklist.docx
Attachment - Clinical Trial Archive Document.docx
Attachment - Clinical Trial Enquiry Form.docx
Attachment - Clinical Trial Enquiry Report.docx
Attachment - Close-out Visit Report Template.docx
Attachment - Contact Comment Form Template.docx
Attachment - CRF Approval Form.docx
Attachment - CRF Completion Guidelines.docx
Attachment - CRF Desing Manual.docx
Attachment - CT Form.docx
Attachment - CTIMP Protocol Template.docx
Attachment - Database Lock Authorisation.docx
Attachment - Declaration of End of Trial Form.docx
Attachment - Disposal Form.docx
Attachment - DMP template.docx
Attachment - Document Retrieval Process Map.docx
Attachment - Document Version Control.docx
Attachment - DSUR Guidance Template.docx
Attachment - eSUSAR User Guide.docx
Attachment - eu-dsur-guidance.pdf
Attachment - Example CPD Record.xlsx
Attachment - Example Personal Training Record.xlsx
Attachment - Fridge Freezer Transfer Log.docx
Attachment - Host Site Initiation Visit Checklist.docx
Attachment - IB Receipt.docx
Attachment - IB TOC.docx
Attachment - ich-dsur-guidance.pdf
Attachment - ISF File Review Checklist Template.docx
Attachment - ISF Index.docx
Attachment - KCL Insurance - Investigator Guidance for CTIMPs.docx
Attachment - Lab checklist.xlsx
Attachment - Mandatory Pages-Adverse Event Log.docx
Attachment - Mandatory Pages-Confirmation of Consent&Demographics.docx
Attachment - Mandatory Pages-Eligibility Review&PI Signature.docx
Attachment - Mandatory Pages-Inclusion&Exclusion Criteria Review.docx
Attachment - Mandatory Pages-Participant Status.docx
Attachment - Mandatory Pages-PI SignOff.docx
Attachment - Mandatory Pages-Trial Completion.docx
Attachment - Mandatory Pages-Trial Medication Administration.docx
Attachment - MHRA Annual Safety Report Template.docx
Attachment - MHRA Guidance on Serious Breaches.docx
Attachment - Monitoring Plan.docx
Attachment - Monitoring Visit Report Template.docx
Attachment - Nitrogen Log.docx
Attachment - Notification of Amendment.docx
Attachment - Notification of Serious Breach examples.docx
Attachment - Notification of Serious Breach Form.docx
Attachment - Optional Pages-CRF Comments Log.docx
Attachment - Optional Pages-CRF Cover Page.docx
Attachment - Optional Pages-Medical History.docx
Attachment - Optional Pages-Physical Examination.docx
Attachment - Optional Pages-Post Randomisation Concomitant Medications.docx
Attachment - Optional Pages-Post Randomisation Laboratory.docx
Attachment - Optional Pages-Post Randomisation Physical Examination.docx
Attachment - Optional Pages-Post Randomisation Visit.docx
Attachment - Optional Pages-Randomisation.docx
Attachment - Optional Pages-Screening Concomitant Medications.docx
Attachment - Optional Pages-Screening ECG.docx
Attachment - Optional Pages-Screening Laboratory.docx
Attachment - Optional Pages-Screening Vital Signs.docx
Attachment - Optional Pages-Smoking&Alcohol History.docx
Attachment - Optional Pages-Unscheduled Visit.docx
Attachment - Pandemic QAs.docx
Attachment - Pharma Amendment Assessment Form.docx
Attachment - Remote Close-out Checklist.docx
Attachment - SAE Reporting Form Guide.docx
Attachment - Sample Log.docx
Attachment - Serious Adverse Event Report Form.docx
Attachment - SIVR template.docx
Attachment - SOP Template.docx
Attachment - Temp Log.docx
Attachment - TMF File Review Checklist.docx
Attachment - TMF Index.docx
Attachment - TMF-ISF Table of Contents.docx
Attachment - Version Control Guideline.docx
SOP - Application Maintenance of a CTA.docx
SOP - Clinical Trials Training.docx
SOP - Computer System Validation.docx
SOP - Creation and Maintenance of Trial Master Files.docx
SOP - CRF Design.docx
SOP - Data Management.docx
SOP - Emergency Code Break.docx
SOP - Informed Consent.docx
SOP - Investigator Brochures.docx
SOP - Laboratory Procedures.docx
SOP - Obtaining Clinical Trial Insurance.docx
SOP - Pandemic Plan.docx
SOP - Pharmacovigilance & Safety Reporting.docx
SOP - Preparation and Submission of Development Safety Update Reports.docx
SOP - Protocol Writing.docx
SOP - Quality Policy.docx
SOP - Sample Management.docx
SOP - Serious Breaches.docx
SOP - Study Setup and Initiation of an Investigator Site.docx
SOP - Vendor Selection.docx
19.下载说明.txt
37.Attachment - Note to File Template.doc
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