About
ur HREC Ethics Coordination service supports sponsors in preparing, organising, and submitting Human Research Ethics Committee (HREC) applications to ensure ethical and regulatory compliance for clinical trials conducted in Australia. We assist pharmaceutical companies, biotech firms, medical device developers, CROs, and academic researchers in preparing clear, comprehensive documentation that meets ethical review requirements. This includes participant information sheets, consent forms, study protocols, investigator documents, risk and safety assessments, recruitment materials, and all supporting evidence required for HREC evaluation. Our expertise ensures your submission is accurate, complete, and aligned with NHMRC guidelines and institutional ethics standards. With structured guidance and document review, you reduce delays, minimise ethics queries, and increase the likelihood of timely HREC approval. Partner with NexaTrials Consulting to streamline your ethics submission process and ensure your clinical trial meets the highest standards of ethical governance and regulatory integrity.