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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.
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  • 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.
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  • HRC Research Ethics Guidelines

    The HRC expects investigators to conduct and report their work with objectivity and scientific honesty.
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  • Monitoring of HRC-funded clinical trials

    The Data Monitoring Core Committee (DMCC) was established to provide objective, independent monitoring of clinical trials funded by the HRC. This flow-chart explains the process.
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  • Pacific Health Research Guidelines 2014

    The following guidelines build on the principles outlined in the HRC’s Guidelines on Pacific Health Research (2005), and address some of the fundamental issues relating to contemporary Pacific health research in an evolving global environment.
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  • Report from an Ethics Committee Seeking Re-Approval

    A Report from an Ethics Committee Seeking Re-approval summarises the activity of the committee over the past three years.
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  • Research involving children

    These Guidelines are based on six principles which are mostly taken from the Guidelines of the Royal College of Paediatrics and Child Health 1999 and the European Convention for the Protection of Human Rights and Dignity of the Human Being with Regard to…
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  • Research involving personal health information

    These guidance notes are provided to assist health researchers and ethics committees, but they should not be relied upon as a substitute for the provisions of the Health Information Privacy Code 1994 (HIPC).
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  • Seeking Ethical Review

    This document outlines when and how to seek ethical review for different types of research.
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  • Standing Committee on Therapeutic Trials (SCOTT)

    The Health Research Council's Standing Committee on Therapeutic Trials (SCOTT) undertakes scientific assessment of applications to conduct trials and makes recommendations to the Director-General of Health on whether or not trials should be approved.
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  • Standing Committee on Therapeutic Trials terms of reference

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