by Admin SDRAN | | SDRAN Events
Wednesday, 17 April 2024 Overview of the Drug Adverse Event Lifecycle Program Speaker: Jacqueline Wright, BSc, RNPharmacovigilance Leader Event Agenda: DATE: Wednesday, 17 April 2024 TIME: 5:30 – 6:00 PM Light Dinner 6:00 – 6:05 PM Welcome...
by Admin SDRAN | | Uncategorized
1. UCI Regulatory Affairs & Compliance for Pharmaceuticals Course 2. UCI Clinical Trials: Medical Device and Drug Development Course 3. UCI Medical Device Development Course...
by Admin SDRAN | | SDRAN Events
EU Clinical Trial Regulation (CTR) and Clinical Trials Information System (CTIS) Program Speaker: Theresa Falls Manager of Regulatory Affairs Avidity Biosciences, Inc. Event Agenda: DATE: Wednesday, 20 March 2024 TIME: 6:00 – 6:05 PM Welcome and...
by Admin SDRAN | | Other Events
Event Details Registration Closed for this event ...
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