The importance of informed consent in clinical research cannot be overstated. Clinical researchers must obtain participants’ consent for their voluntary participation in research. Furthermore, they must explain the purpose and risks associated with the study to participants in a language they can comprehend. The process of creating informed consent documents can be challenging, as it involves meeting several regulatory requirements and understanding the fundamentals of writing informed consent. The webinar delineates these requirements and explains how to effectively write informed consent to meet regulatory requirements and protect participants’ rights and privacy at all times. The webinar also emphasizes the importance of using a laboratory software for clinical research to automate and streamline the management of informed consent.

Who Should Attend?
Recommended attendees include lab managers, directors, quality managers, and technicians of clinical research and clinical trial labs.