CLEAN : Clinical trial death: Biotrial must submit plan of action

The transcript discusses the role of health administration in ensuring volunteer safety in clinical trials. It highlights the need for a defined regulatory framework and the challenges faced in its implementation. An action plan is proposed to improve volunteer safety, with a deadline for submission. The compliance of clinical trials with existing regulations is examined, and the need for enhanced and precise regulations is emphasized. The transcript concludes with a call for regulatory review at the European level.

What is the significance of the agency's role in ensuring the safety of volunteers?

How does the speaker plan to address the issues with the regulations at a broader level?