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A case study evaluation of ethics review systems for multicentre clinical trials

Tania Shelby-James, Meera R Agar and David C Currow
Med J Aust 2010; 192 (5): . || doi: 10.5694/j.1326-5377.2010.tb03514.x
Published online: 1 March 2010

To the Editor: The evaluation by Hicks and colleagues of the centralised ethics review system in New South Wales1 codifies important additional time delays facing researchers conducting multicentre trials that include NSW. These delays have direct financial consequences that continue to limit the viability (especially when staff are on time-limited grants) and productivity of multisite research in Australia, without adding value to the ethical conduct of the research.2 There is also inconsistency between the approaches of the lead ethics committee (LEC) and site-specific ethics committees in the way they deal with protocol amendments and adverse event governance, further compounding the delays in initial review.


  • 1 Department of Palliative and Supportive Services, Flinders University, Adelaide, SA.
  • 2 Braeside Hospital, Sydney, NSW.


Correspondence: david.currow@rgh.sa.gov.au

  • 1. Hicks SC, James RE, Wong N, et al. A case study evaluation of ethics review systems for multicentre clinical trials. Med J Aust 2009; 191: 280-282. <MJA full text>
  • 2. Whiteman DC, Webb PM, Purdie DM, et al. National ethics committee urgently needed. Med J Aust 2003; 178: 187. <MJA full text>
  • 3. Rowett D, Ravenscroft PJ, Hardy J, Currow DC. Using national health policies to improve access to palliative care medications in the community. J Pain Symptom Manage 2009; 37: 395-402.
  • 4. Roberts LM, Bowyer L, Homer CS, Brown MA. Multicentre research: negotiating the ethics approval obstacle course [letter]. Med J Aust 2004; 180: 139. <MJA full text>
  • 5. Hardy J, Shelby-James T, Currow DC. Research in palliative care — is death always an adverse event? Intern Med J 2009. In press.

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