
| The impact of Covid-19 on in-formed consent |
| Informed consent for clinical research in the context of the Covid-19 pandemic between bioethics and biolaw: a general overview |
| Informed consent and group vulnerability in the context of the pandemic |
| Clinical trials in the time of a pandemic: implications for informed consent |
| The ethics of observational/epidemiological research conducted within the Covid-19 pandemic: implications for informed consent |
| Ethical and regulatory issues in vaccine research in the pandemic context and in the case of human challenge studies: implications for informed consent |
| Informed consent, clinical research, Covid-19 and contact tracing apps: some neuroethical concerns |
| Informed consent and artificial intelligence applied to RCT and Covid-19 |
| The bioethical and bio-juridical debate regarding the use of biological samples and data for the purpose of genetic research on human health: open problems |
| How Spanish biobanks have adapted the informed consent process during the Covid-19 pandemic |
| How Covid-19 unveils the blurred borderlines between research and clinical practice monitoring: the use case of data protection and consent |
| Ethical and legal requirements for biomedical research involving health data in the context of the Covid-19 pandemic: is informed consent still playing the leading role? |