News

TPB Submission

Therapeutic Products Bill Submission on impact on clinical trials NZACRes presented the submission in Parliament House on Tuesday 21-Mar-2023 at 3:50pm. The hearings are live-streamed on the Health Select Committee’s Facebook page. Recordings are also posted on their page. Click here for the video...

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Covid 19: Reporting Deviations

The HDEC has provided guidance to NZACRes regarding reporting of protocol deviations/violations during the COVID-19 pandemic. Guidance on protocol deviation/violation reporting had previously been provided to DHB’s but not to the commercial sector. (HDEC meeting communication for DHBs 18-03-20 The...

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Medsafe Standards and Teminology

Medsafe Standards & Terminology The Medsafe document ‘Guideline on the Regulation of Therapeutic Products in New Zealand. Part 11: Clinical Trials – regulatory approval and good clinical practice requirements’ provides the standards and terms that are used by...

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Guidance for New Researchers

Clinical trials can be complicated and nuanced. The more you know, the more you realise there is to know. Fortunately, there is a lot of information freely available online and those who are new to the industry should take full advantage of these resources. Click on the embedded links within this...

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