Question

Clinical studies can be sponsored, or funded, by pharmaceutical companies, academic medical centers, voluntary groups, and other organizations, in addition to Federal agencies such as the National Institutes of Health, the U.S. Department of Defense, and the U.S. Department of Veterans Affairs. Doctors, other health care providers, and other individuals can also sponsor clinical research (Learn About Clinical Studies, 2019). The FDA also plays a big role in clinical trials. To protect and promote health and protect our rights as participants in clinical trials. This includes a series of regulations to monitor clinical trials, which govern elements like (The Role of the FDA, 2019): What must be communicated to patients Consent requirements The data collection process Who can conduct clinical trials Requirements for clinical trial study sites How the process will be monitored The importance of patient privacy Additional protections for children 8 recent clinical trials have been done on diabetes medication in order to understand the link between diabetes and cardiovascular disease (CVD). The FDA would be important in this because they have to approve the drugs. Comment

Answer 1

The FDA is doing a successful job in ensuring proper guidelines are followed in clinical research . However the laws need to be more stringent on who can sponsor these clinical researches. This is because some individual doctors or organizations might misuse it and might avoid following some important rules for which innocent people are becoming victims. Hence the guidelines must be strictly followed and the FDA must ensure the laws are strict enough to stop illegal researches and that researches are being used for a good cause.