WEBINARS
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| FDA Wants Clinical Data to Support Your
510(k); Now What?
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| For more information and to register, click below: |
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| Wed, Mar 3, 2010 12:00 PM - 1:00 PM CST | | | | | | | | | | | | Clinical Evidence Reports (CERs): The Insider's
Guide to Requirements and Process
| | | | For more information and to register, click below: | | | | March 31, 12:00 PM - 1:00 PM CST
| | | | | | | | | | | | Investigator Responsibilities: Protecting the
Rights, Safety, and Welfare of Study Subjects
| | | | For more information and to register, click below: | | | | April 14, 12:00 PM - 1:00 PM CST
| | | | | | | | | | | | Clinical Evidence Reports (CERs): The Insider's
Guide to Requirements and Process | | | | For more information and to register, click below: | | | | May 5, 12:00 PM - 1:00 PM CST | | | | | | | | | | | | An Integrated Approach to CRF Design - Beyond
Clinical Content | | | | For more information and to register, click below: | | | | June 30, 12:00 PM - 1:00 PM CST | | | | | | | | |
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| Check back for more webinar events to come. |
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