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  • Ngå Pou Rangahau - The Strategic Plan for Māori Health Research 2010-2015

    Ngå Pou Rangahau sets out the Måori Health Committee’s vision for Måori health research into the future.
    Resource

  • Statement of Intent

    The Statement of Intent details our strategic direction and desired outcomes over the medium-term and provides performance indicators in order to measure our progress.
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  • Statutory functions of the HRC

    The HRC is responsible to the Minister of Health, and its major funding agreement is through the Minister of Science and Innovation. Our statutory functions are outlined in the Health Research Council Act 1990.
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  • Strategic Refresh of the Health Research Council

    This report of the strategic refresh of the HRC was prepared by officials from the Ministry of Health and the Ministry for Business, Innovation and Employment. It provides ministers with advice on how to maximise the contribution of the HRC to the…
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  • Guidelines for Researchers on Health Research involving Māori

    These Guidelines intend to assist researchers undertaking biomedical, public health or clinical research involving Māori participants or research on issues relevant to Māori health.
    Resource

  • Te Ara Tika Guidelines for Maori Research Ethics

    This document outlines a framework for addressing Māori ethical issues within the context of decision-making by ethics committee members.
    Resource

  • Whaia te Ara Rangahau Hauora Māori - Pathways for Māori Health Research

    This publication provides an overview of the HRC’s activities in Māori health research, and information on the various forms of funding available including career development awards.
    Resource

  • Example Memorandum of Understanding

    This example Memorandum of Understanding (MoU) formalises the intention of the parties to collaborate in a research project and to enter into a sub-contract.
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  • Example Career Development Awards Peer Review Manual

    The CDA Peer Review Manual is specifically for Career Development Award applicants and reviewers. It describes each stage of the review process, the roles of referees, science assessing committees and the HRC Secretariat. For the latest CDA Peer Review…
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  • HRC standard CV template

    This CV template, used by several other organisations, can be used in all HRC funding applications. It standardises the type of information asked for and eliminates the need for researchers to reformat their CV each time they apply for funding.
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  • Example HRC Research Contract

    This example contract covers the agreement between the Health Research Council and a research provider for the duration of a funded research programme.
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  • HRC Rules

    This document outlines the permissible use of research funding and rules around the operation of Contracts
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  • HRC Variation Request Form

    This form is used to provide information to the HRC about proposed variations to current research contracts with the HRC.
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  • Implementing Research - a guideline for health researchers

    This booklet introduces researchers to dissemination and implementation of research, and working with mass media.
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  • Example Peer Review Manual

    The purpose of the Peer Review Manual is to outline each stage of the review process for applicants, committee members and reviewers. For the latest Peer Review Manual pertaining to a specific round, head to the relevant funding page on HRC Gateway.
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  • Review of HRC Funding Decisions, Policy and Procedure

    This policy outlines how the HRC handles requests for a review of funding decisions.
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  • Staff Declaration - HRC Contracts

    This declaration allows Named Investigators and the Contractor to revise and update FTE information, and provides written confirmation that the staff named and paid will be given sufficient workload relief to fulfil the research contract objectives and…
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  • Annual Report from an Ethics Committee

    The HRCEC requires ethics committees to provide an Annual Report from an Ethics Committee, which allows the HRCEC to monitor the activity and functioning of the committee.
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  • HRC Guidelines for Approval of Ethics Committees

    This document sets out the requirements of ethics committees and their governing bodies when gaining approval from the HRC Ethics Committee (HRCEC).
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  • Collection and use of human materials

    There are guidelines and codes governing use of body parts and tissues that differ in the case of living persons and deceased persons, and depending on what the human materials will be used for.
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  • Data Monitoring Committee Charter template

    This document defines the primary roles and responsibilities of a DMC, its relationship with other trial committees, its membership and the purpose, along with a range of other procedural matters.
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  • Data Monitoring Core Committee

    The primary function of the Data Monitoring Core Committee (HRC DMCC) is to ensure that HRC-funded trials that require data and safety monitoring are adequately monitored.
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  • Data Monitoring Core Committee terms of reference

    This document outlines the Committee's scope and responsibilities.
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  • HRC Ethics Committee

    The Health Research Council of New Zealand’s Ethics Committee provides advice on health research ethical issues and the ethical review process.
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  • Ethics Committee Terms of Reference

    This document outlines the Committee's scope and responsibilities.
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  • Ethics in New Zealand – key regulatory bodies

    Beyond the Health Research Council’s committees, there are other important committees and regulatory bodies in New Zealand that contribute to the regulatory environment of health and disability research.
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  • Example of Data Monitoring Committee closed report

    This is an example of a closed meeting Data Monitoring Committee report that contains software generated results.This report uses a random sample of safety data from a randomised clinical trial.
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  • Example of Data Monitoring Committee open report

    This is an example of an open meeting Data Monitoring Committee report that contains software generated results. This report uses a random sample of data from a randomised clinical trial.
    Resource

  • Gene Technology Advisory Committee

    The Health Research Council's Gene Technology Advisory Committee (GTAC) undertakes scientific assessment of clinical trials that involve the introduction of nucleic acids, genetically manipulated micro-organisms, or viruses or cel
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  • Genetic Technology Advisory Committee approval

    Proposals for clinical trials involving nucleic acids may need to seek Genetic Technology Advisory Committee approval.
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  • Gene Technology Advisory Committee terms of reference

    This document outlines the Committee's scope and responsibilities.
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  • Guidelines for Researchers on Health Research Involving Māori 2010

    The HRC's Māori Health Committee has produced these guidelines to assist researchers who intend undertaking biomedical, public health or clinical research involving Māori participants or research on issues relevant to Māori health.
    Resource

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