TAKE ADVANTAGE OF IN-DEPTH HALF-DAY WORKSHOPS ON:

1. Organizing Your Clinical Trial Data for Better Utilization and Decision-Making
2. Meeting the Changing Paradigm for GCP Inspection Readiness

 Address the Shift in FDA Priorities and Enforcement Focus by:

• Driving your business effectively in a new enforcement environment
• Preparing for a collaborative auditing experience between the FDA and EMEA
• Evolving from traditional QA to a quality management culture
• Interpreting and applying the regulatory nuances and ethics of emerging regions
• Ensuring the right mechanisms are in place for effective oversight
• Avoiding over- or under-interpreting the regulations
• Committing to the best processes and smartest use of your resources
• Recognizing compliance gaps across a study or system
• Learning how to look for patterns in deviations and where more training is needed
• Sharing your experiences by actively participating in sessions as well as end-of-day roundtable discussions