This one-day seminar, worth six contact hours/credits, is designed to introduce Good Clinical Practice (GCP)/International Conference of Harmonization (ICH) E6 to clinical research personnel that are new or relatively new to developing products (drugs) for patient care. It is intended to help you begin your preparation to conduct clinical trials in an ethical manner according the regulations and international guidelines. Whether you are a clinical research physician, investigator, study coordinator, or other member of the study team, this program will provide you with the intensive training needed to improve your trials and ensure compliance with Good Clinical Practice, FDA Regulations, and ICH Guidelines.
Get more information about this course, including course objectives, and agenda and staff.