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Juno Research,L.L.C
Delivering High Quality Results
         Juno Research has developed Standard Operating Procedures which: Reduce
    the margin of error. Provide the Coordinators, Investigators and Study Monitors
    with a standard format to easily work with, evaluate and monitor the data collected
    through the study

         We offer study feasibility reports after initial protocol evaluation. This report is
       based
       on study specific inclusion / exclusion criteria and contains the percentage of our
       patient population that are able to potentially enroll. The report also contains the
       numbers of competing studies currently enrolling, possible recruitment strategies
       and our preliminary decision on whether or not we have the means of conduction
       study

         We provide support and management functions to all of our clinical sites
    including:  Contracts and budget negotiation. Regulatory affairs, and recruitment
    planning. This approach allows the Investigator and the Study Coordinators to
    concentrate on conducting the study.

         Our Investigators and Coordinators have ample research experience and have
       previously participated in clinical trials. New Investigators and Coordinators are
       thoroughly trained by senior staff members

       We maintain strict quality controls around our work by regularly evaluating
        our Coordinators and Investigators to ensure accuracy and adherence to
       FDA and GCP guidelines

         Our recruitment procedures allow expedited enrollment times and usually
       enable us to enroll more patients than initially required. Our recruitment
       procedures deliver a 100 % effectiveness rate which guarantees the completion
       of the study on time

       Our main goal is to successfully expedite the approval and marketing of the  
       products  held on Trial.
Specialties
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