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Is Your Study A Clinical Trial
Investigator Initiated Trials
What is an Investigator Initiated Trial?
Test Your Idea
Has your idea been trialled before?
Will Your Clinical Trial Benefit Patients and The Community?
Research Feasibility
Your Research Team
Health Consumer Representatives
Peer Review
Research Impact
Who Needs To Know About Your Clinical Trial?
Research Office and Supporting Departments
Other Affiliated Organisations
Research Involving Aboriginal and Torres Strait Islanders
Culturally and Linguistically Diverse Communities
Clinical Trial Support
Design and Plan Your Clinical Trial
Clinical Trial Design
Demonstrating Research Impact
Clinical Trial Protocol
Trial Safety
Resource Plan and Budget
Source and Confirm Funding
Government Grants
Commercial Entity (Industry) Funding
Non-Government/Philanthropic Funding
Non-government
Philanthropic
Supporting Documentation
Standard Operating Procedures
Files for Essential Trial Documents
Trial Supplies
Identify and Secure A Sponsor
Research Ethics, Governance and Regulatory Approvals
Ethics Applications
Access Request Review for Participants, Their Tissue Or Data
Site-Specific Assessment Application for NSW Public Health Organisations
Therapeutic Goods Administration Application
Trial registration
Site Activation
Trial Management Documents
Qualifications and Credentialing
Insurance and Indemnification
Post Site Activation
Reporting Requirements
Sponsored Trials
I Have A Sponsor and Funding For My Trial
Confidentiality and Feasibility
Confidentiality and Non-Disclosure Agreements
Feasibility Assessment
Site Specific Assessment Considerations
Who Needs to Know About Your Clinical Trials
Research Office- Public Health Organisations
Clinical Trials Support
Other Affiliated Organisations
Agreement Negotiation
Clinical Trial Research Agreements
Budget Negotiations
Memorandum Of Understanding
Research Ethics, Governance and Regulatory Approvals
Ethics Applications
Access Request Review for Participants, Their Tissue or Data
Site Specific Assessment Considerations
Site-Specific Assessment Application- NSW Public Health Organisations
Therapeutic Good Administration Application
Trial Registration
Site Activation
Trial Management Documents
Qualifications and Credentialing
Insurance and Indemnification
Post Site Activation
Reporting Requirements
Home
Is Your Study A Clinical Trial
Investigator Initiated Trials
What is an Investigator Initiated Trial?
Test Your Idea
Has your idea been trialled before?
Will Your Clinical Trial Benefit Patients and The Community?
Research Feasibility
Your Research Team
Health Consumer Representatives
Peer Review
Research Impact
Who Needs To Know About Your Clinical Trial?
Research Office and Supporting Departments
Other Affiliated Organisations
Research Involving Aboriginal and Torres Strait Islanders
Culturally and Linguistically Diverse Communities
Clinical Trial Support
Design and Plan Your Clinical Trial
Clinical Trial Design
Demonstrating Research Impact
Clinical Trial Protocol
Trial Safety
Resource Plan and Budget
Source and Confirm Funding
Government Grants
Commercial Entity (Industry) Funding
Non-Government/Philanthropic Funding
Non-government
Philanthropic
Supporting Documentation
Standard Operating Procedures
Files for Essential Trial Documents
Trial Supplies
Identify and Secure A Sponsor
Research Ethics, Governance and Regulatory Approvals
Ethics Applications
Access Request Review for Participants, Their Tissue Or Data
Site-Specific Assessment Application for NSW Public Health Organisations
Therapeutic Goods Administration Application
Trial registration
Site Activation
Trial Management Documents
Qualifications and Credentialing
Insurance and Indemnification
Post Site Activation
Reporting Requirements
Sponsored Trials
I Have A Sponsor and Funding For My Trial
Confidentiality and Feasibility
Confidentiality and Non-Disclosure Agreements
Feasibility Assessment
Site Specific Assessment Considerations
Who Needs to Know About Your Clinical Trials
Research Office- Public Health Organisations
Clinical Trials Support
Other Affiliated Organisations
Agreement Negotiation
Clinical Trial Research Agreements
Budget Negotiations
Memorandum Of Understanding
Research Ethics, Governance and Regulatory Approvals
Ethics Applications
Access Request Review for Participants, Their Tissue or Data
Site Specific Assessment Considerations
Site-Specific Assessment Application- NSW Public Health Organisations
Therapeutic Good Administration Application
Trial Registration
Site Activation
Trial Management Documents
Qualifications and Credentialing
Insurance and Indemnification
Post Site Activation
Reporting Requirements
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