This new course aims to provide the researcher with the all principles of GCP(Good Clinical Practice) and how they can be applied practically in the research setting.
Course Topics:

 · Why Good Clinical Research and Good Clinical Researcher
 · The Role of Institutional Review Boards/Independent Ethical Committees
 · Informed Consent Documents and Patient Education
 · Confidentiality & Privacy
 · Participant Safety & Adverse Events
 · Quality Assurance
 · Developing Research Protocol
 · Documentation & Record-Keeping
 · Clinical Research Misconduct
 · Roles & Responsibilities
 · Recruitment & Retention
· The Drug Development Process