Forms
The majority of our applications forms are available in Word format only. Guidelines are available in PDF.
Consent and recruitment forms can be found in the Consent and recruitment section.
Please note: our application forms are "locked" documents. In order to initiate typing, place your cursor inside the shaded grey areas.
Long Application Form
This is the standard application form for most projects.
- Long Application Checklist (version date May 2007)
- Long Application for Ethical Approval of Studies Involving Humans (version date May 2007)
The Departmental Impact set reflects the final pages of the Long Application and are separated out here to facilitate transmission and completion by the relevant departments. When completed the corresponding blank sheets in the long application should be removed and replaced with the completed sheets.
- Long Application - Departmental Impact Set (version date November 2006)
Short Application Form
The following application form is for health chart/database research only. If any subject contact is anticipated, or the project will be commercially sponsored, the standard application form must be submitted.
- Short Application for Ethics Approval (version date May 2007)
Data Use Agreement
- Data Use Agreement [Word file - version date January 2008]
- useage guidelines [Acrobat file]
TissueForm
The following application form is for tissue based research only. The tissue may be previously collected or will be prospectively collected.
- Tissue application form (version date May 2007)
Scientific Peer Review
The report on scientific peer review form must be completed and successfully signed off for all applications except for short applications.
- Report on Scientific Peer Review form (version date February 2004)
Adverse Event Reporting
Following study approval investigators must complete an adverse event reporting form for all adverse events, irrespective of the site of the event or its seriousness. Supporting documentation may be attached.
View the reporting guidelines for more detailed guidance.
- Adverse Event reporting form (Word file - version date July 2004)
- Adverse Event Reporting Guidelines (Acrobat file)
Amendment Request Template
Any amendment or modification to an approved study must be submitted and approved prior to activation. Amended consent forms should also be attached, and for major amendments a satisfactory science review must also be attached.
- Amendment Request template (version date June 2003)