This course covers regulatory requirements for conducting clinical trials. It helps you understand and overcome the challenges that arise during the drug development process. This course also helps you understand the importance of Good Clinical Practice (GCP)and the best ways to meet GCP and regulatory expectations to conduct a drug trial.
Upon the completion of this course, participants would be able to:
● Understand the concept and role of clinical trials.
● Describe different phases involved in clinical trials.
● Describe the important regulations and guidelines associated with clinical trials.
Who Should Attend
Students (B. Pharma/ M. Pharma/ B.Sc./M.Sc./ MBBS/ BDS), Industry peers, Regulatory professionals in pharmaceutical and healthcare sectors, academic research centres.