WIB-San Francisco Bay Area Event: What makes a good clinical trial? Moving toward a more interactive, standards-based process

Safety, efficacy, regulatory, oh, my! What are principles of good clinical study design? How do you best execute and monitor a clinical trial? How do you enroll the right patients, and (maybe more importantly) not enroll the wrong ones! Good clinical trials show us the safety and effectiveness of drugs and devices, and WIB-San Francisco Bay Area has invited Ms. Kit Howard, Director of Education at CDISC; Ms. Patricia Kasper, Owner of P. Kasper & Associates; and Ms. Simona Carini, Programmer of UCSF, to an educational panel discussion that addresses these very questions – and more. Our speakers will give us insight into the essentials of clinical study eligibility criteria and study design, explore appropriate and efficient clinical trial monitoring practices, and elaborate on the various regulatory requirements of clinical trials submission to various agencies such as the FDA and EMA.

As always, there will be light snacks, drinks, and time for networking before and after this informative event. We hope you walk away with enlightenment to inform the clinical program at your company. The information presented will be broad ranging and appropriate for all levels.

Register now to reserve your spot. Don’t miss the unique opportunity!

Walk-Ins Will Be Accepted

Cost for Event
Members: $35
Non-Members: $65

Special Pricing for Guests
When registering, members are also allowed 1 guest at member pricing

Maximum Capacity
100

Date/Time
Wednesday, October 29, 2014
5:30 p.m. – 9:00 p.m. PST
(Doors open at 5:30 p.m.; program starts at 6:00 p.m.)