• Clinical Trial Protocol Development
• Clinical Trial/ Project Management 
     Phase I
     Phase II
     Phase III
     Phase IV/ Post Marketing
• Principal Investigator/ Clinical Site Recruitment
• 3rd Party Contract Management

• Consulting Services

• Informed Consent Form Development

• Adverse Event/ Serious Adverse Event Reporting
• IRB Submissions
• Patient Recruitment
• Investigator Reimbursement
• Clinical Monitoring
• Medical Writing
• FDA Submissions:
     IND
     NDA
     FDA 1571