Talk to Julie about these topics and more:  

• Human research protection regulations  
• Site operations of clinical research  
• Next-generations IRBs  

Talk to Mark about these topics and more: 

• Clinical trial technology solutions 
• Clinical analytics 
• Open-source solutions for clinical data 
• Using SAS and R in symbiotic ways for clinical trial data 

Talk to Jay about these topics and more:

• Understanding cardiac safety requirements, including protocol design 
• Sponsor support at FDA meetings 
• Early phase development 
• Working with data and safety monitoring boards 
• Cardiac arrhythmias and electrophysiology  

Talk to Cassie about these topics and more:

• Navigating U.S. regulatory requirements, IND Submission, and Phase 1 startup and conduct 
• Efficiencies and guidance in running Phase 1 of clinical development  
• Understanding cardiac safety requirements and the best cost-saving methods 
• Developing new service programs as needs emerge 
• Rapid operational scaling/growth, strategic planning, and recapitalization