Following up on my last few posts on the importance of informed consent in medical research, I wanted to dig deeper into the practice of clinical trials and patients' rights in medical research. The concept of informed consent, the basis of which is the stipulation that people will make the right choice for their own health and wellness, is a well-established principle of bioethics. However, it is less clear about its prevalence in public health, and the recent covid-19 pandemic has further stoked discussions about patients' rights and value of consent in the face of a global health event. The DNA genetic testing company, 23andMe, has also demonstrated how consent is an obstruction to researchers’ ability to use and exploit personal data. It is known that the company's primary goal is to gather genetic data that can then be used for research. However, the company has feined an interest in empowering individuals to take control of their own health, and used that for their ma
Blog on the History of Medicine and Medical Science from the Ancient Times to Modern