
Before any new drug or medicine can be bought to market, the Sponsor or Developer must prove the drug does what it is intended to do, all side effects are known and understood, and it is safe for humans to take. This article outlines the clinical research processes and checks NZCR must follow to ensure trials are conducted safely and ethically.

New Zealand Clinical Research (NZCR) undertakes clinical trials in NZ for many medical and pharmaceutical groups around the world. This must be done under strict regulatory controls to ensure the medical trial is conducted safely, ethically, and with scientific rigour. Learn about the meticulous review process NZCR must undergo before they can start trialing any new drug.

New Zealand Clinical Research (NZCR) is a leading early-phase clinical research provider. Our expert research team has conducted over 750 clinical studies in NZ involving more than 15,000 New Zealanders. With facilities in Wellington, Hamilton, Christchurch, and Auckland, clinical trials are being conducted daily to test investigative medicines. For NZCR to do this research it needs healthy people and patients to join its research community.

The life of a participant in clinical trials in NZ gives individuals the opportunity to take part in research that could improve many people's lives. Participating in a clinical trial in NZ can vary depending on the type of trial and its objectives, and medical trials can be from one day to up to 18 days with follow-up visits.

Clinical trials in NZ are designed to advance global health, and usually are part of a multi-country trial approach. At NZCR , our clinical research teams’ partner with leading medical researchers, doctors and science experts to help develop innovative medicines and treatments that improve people's lives.