Research at Adventist HealthCare
Clinical Trials Information
Clinical Trials through the AHCL Research & Ethics Office
The opportunity to be involved in Clinical Trials as part of projects approved by the Research Office can be facilitated where appropriate.
Information on specific clinical trials can be found by searching the following sites:
San Clinical Trials Unit
The San Clinical Trials Unit (CTU) is a not-for-profit organisation that is part of the Adventist HealthCare group. We are made up of a team of Medical Oncologists, Clinical Trial Coordinator’s, Clinical Trial Pharmacists and experienced Oncology Nurses. Our purpose is to provide all Oncology patients treated at Sydney Adventist Hospital the best possible treatment outcomes through offering them the opportunity and ability to participate in the most current treatment options available in this field.
Information for Researchers Interested in Conducting a Clinical Trial
- https://www.australianclinicaltrials.gov.au/
A joint initiative between the National Health and Medical Research Council and the Department of Industry, Innovation and Science to provide information and resources to consumers, health care providers, researchers and industry about clinical trials. - https://www1.health.gov.au/internet/main/publishing.nsf/Content/Clinical-Trials
Australian government departments, committees, and industry stakeholders to progress improvements to the clinical trial environment. - https://www.tga.gov.au/clinical-trials
Regulation of the use of therapeutic goods supplied in clinical trials in Australia under the therapeutic goods legislation - https://www.medicinesaustralia.com.au/policy/clinical-trials/
Access to contract templates and indemnity and compensation guidelines for clinical trials involving DRUGS in Australia - Clinical Trials in Australia - MTAA
Medical Technology Association of Australia - Access to contract templates and indemnity and compensation guidelines for clinical trials involving DEVICES in Australia - https://www.nhmrc.gov.au/about-us/publications/safety-monitoring-and-reporting-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.