GCP Seminar Course Details

More and more sponsors are requiring Investigators and Coordinators in clinical research to have formalized, documented training in GCP and FDA regulations, but these seminars are far and few between and worse, they are often very expensive!

Inexpensive Partnered Training

Clinical Trials of Texas, Inc. and Barnett Educational Services have partnered together to provide an affordable training seminar in South Central Texas that will meet sponsor requirements as well as provide CEUs for applicable attendees.  This is a one-day training course conveniently taking place on a Saturday (October 20, 2007). Breakfast, Lunch and snacks throughout the day will be provided and included in the registration fee.  This is our first attempt to provide this training, and we hope to have a large turn-out to justify recurrent training on an annual basis.  Please see the Course Agenda as well as the very affordable Registration.

Course Agenda Introduction to GCP Informed Consent Process Clinical Research Team Members: Roles and Responsibilities Safety Reporting Source Documentation Financial Disclosure Clinical Investigator Site Audits and Regulatory Inspections Course Evaluation / Q&A

Attendance Information Date: October 20th, 2007 Time: 8:30am - 5:00pm Location: Doubletree Hotel 37 NE Loop 410 San Antonio, TX 78216 Registration: Investigators: $400.00 each Clinical Staff: $400.00 each Double Tree offers room discounts for attendees Late registration fees will apply after September 30 Registration fee includes: GCP Training Certificate, Comprehensive Course Materials, 7.5 Hours/.75 CEUs through ACPE & Nursing CEUs, Breakfast, Lunch, Snacks

Course Goals

Our goal is to make this a successful, educational, and relaxing seminar that will enhance you and your entire staff’s knowledge of Good Clinical Practices and FDA regulations in the clinical research setting.  We look forward to seeing you at the beautiful Double Tree Hotel in San Antonio!