HUMAN RESEARCH ETHICS DOCUMENT SERVICES

Planning  •  Preparation  •  Submission Planning  •  Preparation
Submission

Ethicsready is the culmination of 30 combined years in Clinical Trial Coordination, Clinical Trial Administration, Ethics Coordination and Compliance Officer experience. Ethicsready professionals have worked across Sponsored, Collaborative Group and Investigator Initiated Clinical Trials in Human Research.

Ethicsready has been developed to provide Sponsors, Contract Research Organisations (CRO), Clinical Trial Sites and Investigators with practical guidance, document content development and Human Research Ethics Committee (HREC) submission preparation and/or submission services.

Ethicsready streamlines the ethical administration of research whilst complying with all applicable Ethical and Regulatory guidelines.