Take aggressive steps when preparing for clinical trials and conducting clinical research to ensure GCP compliance and find any trial vulnerabilities prior to FDA audits. Attend this advanced training to:

Hear the NIH Roadmaps vision and how it affects current and future clinical research
Utilize GCP in clinical trial protocol design
Understand the importance of selecting an appropriate trial design that assists in remaining GCP compliant
Write and manage SOPs to ensure clinical quality assurance
Explore onsite monitoring techniques
Discover methods to prevent clinical investigator and patient non compliance
Optimize clinical trial data collection and integrity to maintain FDA compliance