Documents and templates

Back to Running a study

Our documents and templates are provided below. If you would like to see our standard operating procedures please click here.

Title	Description
Remove
Adverse Event Reporting (Not SAE, SAR, SUSAR) FRM005.doc	FRM005
Adverse Events Reporting (SAE, SAR, SUSAR) FRM007.doc	FRM007
Archive Retrieval Form FRM059.docx	FRM059
Audit Report FRM025.docx	FRM025
Certificate of Destruction FRM060.docx	FRM060
Charter for Trial Management Group with Independent Chair TPL016.doc	TPL016
Check List for eSAE CRF Design FRM055.xlsx	FRM055
Clinical Code Break Request Form FRM029.doc	FRM029
Clinical Data Management Study Set up GD007.docx	GD007
Clinical Data Management Validation GD014.docx	GD014
Codebreak Test procedure FRM030.docx	FRM030
Data Amendment FRM002.xlsx	FRM002
Data Cleaning GD012.docx	GD012
Data Management Plan GD016 v1.0.pdf	GD016
Data Validation Plan FRM048.xlsx	FRM048
Database Lock and Close Down FRM017.docx	FRM017
Database Testing Validation and Acceptance FRM018.docx	FRM018
Database Training Data Entry Training FRM015.docx	FRM015
Database Unlock Request FRM019.xlsx	FRM019

Back to Running a study

Where are we based?