1-Day In-person Seminar (January 14, 2016)
Risk Management in Clinical Studies
Risk management in clinical trials involves identifying, reducing and monitoring risks to patient safety, data integrity, regulatory and protocol compliance, and project scope (budget and timelines). By properly assessing risk and applying the most appropriate monitoring strategy according to risk priorities, threats to patient safety and data integrity can be foreseen and either avoided or mitigated because they are caught early. It is important to factor in risk into all trial activities and continuously address it through all stages of trial execution.
With this one-day training, we hope to impart the knowledge that is needed by a clinical trial professional to manage risk in the real world. The training would be carried out by instructors who have wealth of experience successfully managing risk in clinical trials. The tips that the instructors will share during the course of the training program will be invaluable, regardless of where you are in your career.
Who Will Benefit:
For additional information on the workshop agenda and logistics, please call +1 877-566-4981 or +1 410-501-5777 or email: firstname.lastname@example.org