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.

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