Registration and Reporting

Registration and Reporting

The World Medical Association Declaration of Helsinki states that “Every research study involving human subjects must be registered in a publicly accessible database before recruitment of the first subject”

If your study is a Clinical Trial of an Investigational Medicinal Product (CTIMP), designed to assess the efficacy of a healthcare intervention, results must be uploaded to the EudraCT database.

The International Committee of Medical Journal Editors' (ICMJE) considers randomised clinical trials for publication only if registered in an appropriate registry, with an aim to stop selective reporting of positive trials and allow the many stakeholders in clinical research to explore a full range of clinical evidence.