1.   Documents placed in review and are lost… requiring

               additional time, energy and capital
    2.   Inefficiencies due to inability to monitor who is making

               changes to what documents
    3.   Long turnaround time for documents in review causing

               unnecessary delays
    4.   Compliance to FDA, ISO, SEC, OSHA, HIPPA, 21 CFR Part

               11 and other regulatory standards
    5.   Excessive time spent copying documents and updating

               necessary procedure binders
    6.   Important information is not readily accessible.

              (Seek and find Missions)
    7.   Inability or difficulty verifying personnel training
    8.   Inability or difficulty locating data due to manual formats

               or multiple databases
    9.   Multiple groups revising the same document causing

               confusion, inefficiency and lost data
    10. Stressful when preparing for audits due to inefficiency in

               data organization
    11. Ineffective in notifying appropriate personnel of revised

               pertinent information
    12. Inefficient method of recording training information
    13. Lack of automated quality processes result in duplication

              in work and communications
    14. Excessive cost for performing manual processes
    15. Communication breakdown due to sharing information

               between multiple locations
    16. Other (please describe)

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