Research teams are required to advise the Eye and Ear Research Office of any amendments to the approved project. This refers to projects approved by:

  • Eye and Ear site specific research governance

Refer to the information below for instructions related to:

Amendments (including changes to members of the research team)

Annual Progress, Safety and Final Reports

All research projects are monitored annually with a Progress Report and a Final Report at the completion of the project.

Some research projects may require more frequent reporting or additional reporting.  Please refer to the letter of governance authorisation regarding any specific reporting requirements.

Monitoring and Safety Reporting (Adverse Events and Breaches)

The Eye and Ear has adopted the following guidelines from 1 April 2019

  1. NHMRC Guidance: Safety monitoring and reporting in clinical trials involving therapeutic goods (NHMRC; November 2016)
  2. NHMRC Guidance: Risk-based management and monitoring of Clinical Trials involving Therapeutic Goods (NHMRC; 2018)
  3. NHMRC Guidance Reporting of Serious Breaches of Good Clinical Practice (GDP) or the Protocol for Trials Involving Therapeutic Goods (NHMRC; 2018)
  4. NHMRC Guidance Data Safety Monitoring Boards (DSMBs) (NHMRC; 2018)

All guidelines are available from the NHMRC website.

The Eye and Ear Monitoring and Safety Reporting of Research Projects Procedures (including a summary table) have been reviewed and updated and apply from 23 October 2019.