Documents and templates

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

Title	Description
Adverse Events Reporting (SAE, SAR, SUSAR) FRM007.doc	FRM007
Archive Retrieval Form FRM059.docx	FRM059
Certificate of Destruction FRM060.docx	FRM060
Clinical Data Management Study Set up GD007.docx	GD007
Codebreak Test procedure FRM030	FRM030
Data Cleaning GD012.docx	GD012
Database Lock and Close Down FRM017.docx	FRM017
Database Training Data Entry Training FRM015.docx	FRM015
Database Validation Specifications FRM016.xlsx	FRM016
Development Safety Update Report FRM045.rtf	FRM045
Drug Accountability Log FRM031.docx	FRM031
End of Study Sample Declaration FRM069.docx	FRM069
Form Returns slip for IMP returns v1.0.docx
FRM005 Adverse Event Reporting (Not SAE, SAR, SUSAR)	FRM005
FRM012 Version Control of Trust Approved Document	FRM012
FRM018 Database Acceptance Form	FRM018
FRM019 Database Unlock Request	FRM019
FRM021 Sponsor File Index	FRM021
FRM025 Audit Report	FRM025
FRM029 Clinical Code Break Request Form	FRM029

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