Learn how Informed Consent is recorded from Clinical Research Courses?

How do patients usually arrive at the decision regarding informed consent?

Clinical research courses

What are the 2 ways in which consent is recorded?

PG Diploma in Clinical Research

1. Paper consent

Paper consent is collected in person by a professional from the participant of the study or trial.


2. electronic consent (eConsent)

Electronic consent or eConsent primarily uses hyperlinks, videos, and assessment tools to help with interpreting the consent document.


Yet, the professional still would confirm that the entire process of informed consent is complete with the assistance of other professionals. The information is usually reviewed by a physician or by researchers with appropriate scientific training and qualifications. Thus, it becomes essential for professionals to follow the rules effectively and they can learn the rules and regulations from clinical research courses.

Making the Process Simpler for the Participants

Most participants may not have a science or medical back ground hence they may ask a lot of questions. It is up to the professionals on how they make it simpler and that is why they should implement the suggestions given in clinical research courses.

https://www.technobridge.in/clinical-research-course.html

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