Julie Jones, Author at NZACRes

Members New Zealand

June 21, 2021

Medical Technology CIRA’s updated

Sponsor & CRO MedTech sCIRA's Updated - June 2021 The Sponsor and CRO Medical Technology Standardised Clinical Investigation Research Agreement's have been updated to remove the reference to the Medicines New…

Julie Jones

Love502

Members New Zealand

May 26, 2021

The Maori Consultation Process

Overview of the Maori Consultation Process A good place to start regarding cultural requirements for completing the HDEC application is the HDEC website, HRC guidance and NEAC guidance: https://ethics.health.govt.nz/guides-templates-forms-0/cultural-questions-hdec-application-guidance https://www.hrc.govt.nz/resources/guidelines-researchers-health-research-involving-maori…

Julie Jones

Love502

NZACRes

May 16, 2021

NZACRes Newsletter May 2021

The NZACRes committee released newsletter 04, May of 2021. The May 2021 edition highlights the new members website section, registration changes and event ticketing abilities. NZACRes is also offering free…

Julie Jones

Love502

Historical New Zealand

April 10, 2021

Consultation – Medsafe Fees Review

Closes 7 May 2021 Opened 8 Apr 2021 The consultation document provides proposals on changes to Medsafe fees by way of improved and targeted cost recovery of evaluation and licensing…

Julie Jones

Love502

Members New Zealand NZACRes

March 15, 2021

HDEC Application Tips

The HDEC Application Tips document provides advice to optimise your chance of gaining Health and Disability Ethics Committee (HDEC) approval. It also highlights issues and errors that the HDEC's commonly…

Julie Jones

Love502

International New Zealand

January 10, 2021

NZ a promising destination for trials in a post-Covid-19 world?

PharmaceuticalTechnology.com By Allie Nawrat 17 December 2020 (Last Updated December 17th, 2020 20:58) Unlike the rest of the world, New Zealand’s speedy and decisive response to Covid-19 has successfully enabled…

Julie Jones

Love502

New Zealand NZACRes

November 2, 2020

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…

Julie Jones

Love502

New Zealand NZACRes

August 24, 2020

Guidance for New Researchers

New to Research? – Don’t reinvent the wheel! Clinical trials can be complicated and nuanced. The more you know, the more you realise there is to know. Fortunately, there is…

Julie Jones

Love502

NZACRes

August 14, 2020

NZACRes Newsletter August 2020

The NZACRes committee has released it's third newsletter of 2020. The August edition contains a number NZACRes news items, information regarding the new and updated HDEC PISCF templates, industry reports…

Julie Jones

Love502

NZACRes

August 9, 2020

Consultation – standard indemnity

NZACRes is conducting a consultation regarding our template standard Indemnity & Compensation Agreement (sICA) Please contact us at info@nzacres.org.nz if you would like to provide feedback on the sICA or…

Julie Jones

Love502

Julie Jones

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