Ethics & research governance library

Easy access to our ethics and governance forms and research guidelines.

Clear filter
Resource title Size Resource type
Pharmacy service research request form 119 KB Forms & templates
Post COVID-19 clinical trial report 26 KB Forms & templates
Poster Printing Checklist
Poster design and printing checklist for research poster displays.
423 KB Guidelines & checklists
PrEPX consent form
Study consent form
728 KB Forms & templates
PrEPX South Australia consent form 350 KB Forms & templates
PrEPX Tasmania: Patient information and consent form
Important patient information and consent form to be completed by prospective participants.
2 MB Forms & templates
Progress report - project form
Report for the Ethics Committee on all approved sites
87 KB Forms & templates
Progress report - site form
Used by Alfred Health sites to report to Alfred Health governance
86 KB Forms & templates
Progress reporting scenarios table 537 KB Information
Project final report & site closure report 86 KB Forms & templates
Projects granted a waiver 258 KB Information
Protocol for research utilising resected or biopsied tissue 463 KB Guidelines & checklists
Quick reference table 476 KB Information
RACC notice to conduct research 48 KB Forms & templates
Radiation services guideline for clinical trials 33 KB Information
Radiology e-order guideline 1 MB Guidelines & checklists
Radiology trial services guidelines
Diagnostic services, procedure fees, online form guide, image download guide
1 MB Guidelines & checklists
Reporting of Serious Breaches of Good Clinical Practice (GCP) or the Protocol for Trials Involving Guidelines & checklists, Policy, Website
Research collaboration agreement 291 KB Forms & templates
Research Day Flyer 641 KB
Research funding contract checklist 35 KB Guidelines & checklists
Research Governance checklist 603 KB Guidelines & checklists
Research Poster Template 115 KB Forms & templates
Research: Referral of Issue for Discussion form 36 KB Forms & templates
Safety monitoring and reporting in clinical trials involving therapeutic goods
This document clarifies the responsibilities of those involved in clinical trials to monitor and report adverse events and other safety issues. Supplementary guidance on other clinical trial safety monitoring and reporting issues is also available.
Guidelines & checklists, Policy, Website
Safety report form 77 KB Forms & templates
Scientific reporting template 30 KB Forms & templates
Self audit tool 158 KB Forms & templates
Serious breach report form 91 KB Forms & templates
Site Questionnaire: Radiology dept imaging capabilities form
Provide this form to the sponsor
375 KB
Sleep laboratory service research request form 302 KB Forms & templates
Small Project Grants Application Form 52 KB Forms & templates
Small Project Grants Guide 158 KB Guidelines & checklists
SPG Flyer 2017 121 KB Information
Standard wording for PICFs 268 KB Information
Suspected breach report form 81 KB Forms & templates
Tele-trial Subcontract - MA CTRA 53 KB Forms & templates
Template A 38 KB Forms & templates
Template B 46 KB Forms & templates
Terms of Reference Ethics Committee 167 KB Information
Terms of Reference Research Ethical Issues Sub-Committee 46 KB Information
Terms of Reference Research Review Committee 55 KB Information
The Alfred Book of Abstracts 2018
Abstracts from Research Week 2018
2 MB Information
The Alfred Brain Tumour Access Policy 222 KB Policy
The Alfred Neuroscience Biobank - data & sample request form 191 KB Request form
TrialHub’s impact brochure 1 MB Information
Update GCP training 276 KB Information
Update ICH GCP E6 R2 200 KB Information
Update safety monitoring 250 KB Information
Updated Alfred Health COVID-19 guidance for onsite monitoring 232 KB
1 2 3 4