Medical device clinical research training online is now available.
CHICAGO, IL (PRWEB) April 21, 2004 -— Clinical Device Group Inc announced today that it has acquired state-of-the-art technology that allows the company to deliver online clini-cal research training to meet FDA requirements. This virtual classroom" allows for interactive discussions, real time exercises, break-out sessions and case studies, providing an ideal opportunity to benchmark, network, and interact with colleagues without the travel constrains present in many companies today. Some sessions are complimentary; others are pay-per-registration. The current schedule can be viewed at http://clinicaldevice.webex.com .
The clinical research webinars focus on medical device clinical research both in Europe and in the US. Topics include: Applied Regulations, Good Monitoring Prac-tices, Clinical Trials Design and Project Management for Clinical Trials; and focus on FDA, 21 CFR Part 812, ISO 14155, IDE submissions, FDA inspections, monitoring in-vestigational sites, data management, statistical, study design, protocol organization, and other clinical research issues relevant to conducting successful studies.
About Clinical Device Group Inc
Clinical Device Group, founded in 1990, monitors clinical research practices within the medical device industry. In addition, they are a consulting and contracting firm for medical device clinical research and biological safety. The owner, Dr. Nancy J Stark, has published numerous books and articles on clinical research and conducts around 20 public and private training courses each year.
For further information, please contact Maria Sikirica at 1-773-489-5706 or cdginc@clinicaldevice.com, or visit www.clinicaldevice.com.
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