The Coalition on Reducing Bureaucracy in Clinical Trials, in which BioMed Alliance is an active member, just published a series of concrete and consensus-based recommendations for reducing administrative burdens in clinical trials. The recommendations reflect the needs and perspectives of investigators and patients, but are also taking into account the views of regulators, sponsors, ethics committees and other stakeholders to ensure the broadest possible uptake of the proposed the solutions.

The recommendations are gathered in four clusters: safety reporting, informed consent, regulatory guidelines and harmonisation of requirements accross the EU.

The Coalition Recommendations are available for reading on the website of the Coalition here.