ProIRB^®
                        for the IRB professional

• Creates a more professional image surrounding Review Board activities and responsibilities.
  
  
• Allows you to track your Principle Investigator activities and responsibilities.
  
  
• Reduces risk and speeds up the Informed Consent review process.
  
  
• Helps you stay ahead of and automatically track Revised Consent forms.
  
  
  
• Allows you to make sure we receive progress reports before we allow a Study to continue.
  
  
  
• · Makes certain your board is current on the latest revisions to the Study.
  
  
  
• Streamlines the process of in house audits.
  
  
  
• Speeds the entry of data and prevents the duplication of PI, Sponsor, and Coordinator data.
  
  
• Easily accommodates ad hoc information requests that would otherwise be too time consuming or impossible to generate.
  
  
  

CyberIRB^®
                        the next generation

• Dramatically increases support for and facilitates the quality, accuracy and timelines of IRB action.
  
  
• Enhances IRBs ability to provide substantive and meaningful review of research studies upon inception and then throughout the research process.
  
  
• PI has access to only the most current approved Consent Forms.
  
  
• More effective use of IRB staff to review and research submissions rather than to input data.
  
  
  
• IRB Members can review Protocol history and Adverse Events prior to meeting.
  
  
• Enhances IRBs in insuring the rights and welfare of human research.
  
  
• Reduces the sheer volume of hard copy documents.
  
  
• Increases timelines and accuracy of submissions via point of entry edit by PIs.
  
  
• Standardized communications help familiarize all with regulatory guidelines.

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