requirements for conducting clinical

The Clinical Trials Regulation sets out specific requirements for conducting clinical trials involving human subjects. Article 28 of this regulation focuses on informed consent, mandating that participants must be fully informed of the objectives, risks, and benefits of the trial before they can participate. For biohackers engaging in any form of human experimentation, particularly in the realm of medical devices or novel health interventions, compliance with this article is essential to ensure that ethical standards are met. Furthermore, Article 35 establishes provisions for vulnerable populations, such as individuals with reduced autonomy, who may be more susceptible to harm from risky biohacking experiments. สล็อตเว็บตรง