Spring, 2008 for Charlotte, NC, Columbia, SC or Greenville, SC.  Specific Date and Location Coming Soon.

Description - This course is an extensive training program for clinical research coordinators and investigators, and provides many helpful tools and techniques that are directly applicable to their roles in clinical research. The curriculum is designed to provide a strong foundation in Good Clinical Practices and medical ethics. 
                                                                                           
Class Agenda/Modules -                                  Instructors Make a Difference

• Good Clinical Practices
• Master Drug Accountability
• Protocol and Investigator’s Brochure
• Human Subject’s Protection
• Monitoring Visit Process
• CRC Macro Skill-Set
• CRC Micro Skill-Set
• Adverse Event Reporting
• Successful Regulatory and Client Audits
• Sensitivity to Scientific Misconduct

Typical Class Attendee -

• Clinical Research Coordinators
• Clinical Investigators
• Clinical Research Directors
• Site Clinical Research Quality Assurance Auditors

Coordinator Level - Beginner to two years of experience, or experienced professionals in need of formal training

Class Price - $300 for One-Day Introductory Class.

$600 for Two-Day Complete Class

(additional 5% discount for 2 or more persons  from the same organization)