Duration : 1 Day
Time : 9 AM – 5 PM
This course is aimed to introduce the concept of Good Clinical Practice in Clinical Research. The key elements of the ICH Good Clinical Practices will be discussed, including the ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects. You will be able to demonstrate a good understanding of the ethical principles related to clinical trial, understand the meaning of “protection of the rights, well-being and safety of the trial subjects”, be able to list all the essential documents required to collectively permit evaluation throughout the conduct of a trial and the quality of the data produced, and be able to understand the roles and responsibilities of an investigator, a sponsor, a Clinical Research Organization, the Research Ethics Board and the subjects in a clinical trial.
Who should attend?
A, QC, Regulatory Affairs, Production and Distribution
- Medical / Nurse Practitioner
- Clinical Investigator
- Clinical Research Associate
- Research and Development (R&D), Analytical Development (AD)
25 Watline Ave, Suite #201, Mississauga, ON, L4Z 2Z1