Course "Designing and Monitoring Approvable Medical Device (cardiovascular) Protocols" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.Overview: Construction of an approvable clinical trial protocol requires excellent scientific writing and organization skills. Also paramount is gathering necessary information to manage the statistical analysis and data management of the study. This usually starts with a literature review, establishing key efficacy and safety parameters and determining proper sample size. Sample size calculations are a very important aspect of clinical trials, as are the consent and data collection forms, therefore the statistics and data management departments must be included for their input into the protocol and timelines.Location: Los Angeles, CA Date: April 21st & 22nd 2016 and Time: 9:00 AM to 6:00 PM Venue: DoubleTree by Hilton Hotel Los Angeles Downtown Address: 120 South Los Angeles Street, Los Angeles, California, 90012, USA Price: Register now and save $200. (Early Bird)Price: $1,295.00 (Seminar for One Delegate)Until March 10, Early Bird Price: $1,295.00 from March 11 to April 19, Regular Price: $1,495.00Quick Contact:NetZealous DBA as GlobalCompliancePanel  Phone: 1-800-447-9407Fax: 302-288-6884