Upcoming Courses
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$299
Quality Management of Electronic Systems in Clinical Trial Investigations: A Comparison of FDA and EMA GuidanceSandra “SAM” SatherJuly 30, 2020 | 1 PM EDT -
$299
Regulatory Affairs in China – The New Drug Regulatory FrameworkMichael Zhang, Katrin RupallaJuly 16, 2020 | 1 PM EDT -
$179
Critical Documentation of Clinical Trial Activities and CAPA During and Post COVID-19 RestrictionsSandra “SAM” SatherOn-Demand -
$299
FDA REMS Inspection Guide: Audit Preparedness Best PracticesPenelope Przekop, MSQA, RQAP-GCPJuly 28, 2020 | 1 PM EDT -
$279
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$299
Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAsPenelope Przekop, MSQA, RQAP-GCPTBD -
$299
Executing Proper Event Investigations: Critical Steps In Ensuring Compliant Corrective ActionsJudy Carmody, Ph.D.July 9, 2020 | 1 PM EDT -
$299
Measuring CAPA Effectiveness: Critical Tips in Getting the Right CAPA and Showing It WorksJoanna GallantJuly 15, 2020 | 1 PM EDT -
$299
The Top Method Validation Mistakes – And How to Avoid ThemJudy Carmody, Ph.D.July 23, 2020 | 1 PM EDT