In Clinical Research Courses Learn how Informed Consent is recorded
How do patients usually arrive at the decision regarding informed consent? In the process of informed consent, doctors or even professionals from the clinical research industry provide patients information on a specific test or treatment, Clinical research courses advice students on how they can suggest certain treatments or tests to patients. Once professionals give the patients this information, patients can then take a decision on whether they want to go ahead with the treatment or not. This is usually how the process of informed consent takes place and that’s why it is covered in a detailed manner in clinical research courses such that it is done in a proper manner. What are the 2 ways in which consent is recorded? There are 2 different ways in which the process of informed consent takes place and is recorded by professionals. Clinical research courses cover both procedures namely on paper and in electronic format. Apart from that, there are different components...