Question

Discuss the benefits of blinding, randomization, and having a control group. Should this be required for FDA approval studies?

300 words no bullet points no plagiarism Thanks

Answer 1

Benefits of blinding, randomisations and control group:

Researchers who  decide randomly as to which participants in the trial receive the new treatment and which receive a placebo, or fake treatments is called randomisation. This is to determine the group receiving the active treatment if they look more likely to benefit from the experimental treatment or not. Randomization removes bias and truly allows for a direct comparison between two groups in a trial, providing a real representation of how the drug will react with the wider population after distribution. This is basically experimental methods towards the treating and development of new and advanced medications.through examination of the trial treatment or drugs with great precautions both legally and clinically.control group is where the people who are the participants do not receive the new treatment but instead receive a placebo or reference treatment. Fake or dummy treatment that closely resembles the experimental treatment but does not contain the active ingredient that causes the treatment's supposed benefits.yes, food and drug administration should approve the study.