Auditing Clinical Trials for GCP Compliance
Training Overview
Improve Your Ability to:
- Audit clinical trials for adherence to Good Clinical Practice (GCP) regulations and run a compliant and efficient clinical trial
- Identify and avoid the consequences of non-compliance, misconduct and fraud to avoid costly delays
- Review common pitfalls within clinical trials and recognize potential problem areas before it is too late
- Write, implement and update Standard Operating Procedures (SOPs) to establish a solid backbone to your auditing program
- Develop tools for auditing internal clinical files, clinical sites and clinical data and improve your auditing ability
- Master interviewing skills to effectively obtain necessary information from clinical sites
- Complete a clinical data trend analysis—an early warning teller of potential problems
- Document findings properly in an audit report and provide management with a clear understanding of your audit
- Ensure compliance with informed consent requirements and HIPAA privacy rule
- Select and qualify vendors to ensure outsourced areas meet regulatory standards
- Anticipate, prepare for and manage FDA inspections so you never get caught off guard
PTi international is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmaceutical education. Participants will receive a maximum of 14 hours (1.4 CEUs) of continuing education credit for full participation in the two-day training. ACPE # 326-000-06-014-L04. Initial release: 07/2006.
Booking Options
Booking Options:
- Register online or Call Customer Service - Tel: (866) 647-0921 or email register@pti-international.com
- Group Discounts (3 or more people for this course) - Call your Course Guidance Manager at (646) 895-7447 or email CourseManager@pti-international.com
- Bring this Course to Your Facility (10 or more people or further customization) - Call (800) 303-8194 or email OnSiteSolutions@pti-international.com