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Webinar
The Participant Playbook Webinar Series, Part 3 — Rethinking the Development of Participant-Centric Clinical Trial Technology
Apr. 12, 2023
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Apr. 12, 2023
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Conference
Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials
Apr. 25, 2023
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Apr. 27, 2023
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Conference
FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know
Apr. 26, 2023
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Apr. 26, 2023
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Webinar
Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis
Apr. 27, 2023
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Apr. 27, 2023
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Conference
2023 WCG Avoca Quality Consortium Summit
May 17, 2023
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May 18, 2023
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Conference
WCG MAGI Clinical Research Conference – 2023 East
May 21, 2023
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May 24, 2023
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Upcoming Events
12
Apr
The Participant Playbook Webinar Series, Part 3 — Rethinking the Development of Participant-Centric Clinical Trial Technology
25
Apr
Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials
26
Apr
FDA’s New Laws and Regulations: What Drug and Biologics Manufacturers Need to Know
27
Apr
Califf’s FDA, 2023 and Beyond: Key Developments, Insights and Analysis
17
May
2023 WCG Avoca Quality Consortium Summit
21
May
WCG MAGI Clinical Research Conference – 2023 East
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Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant
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Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials
The information you need to adapt your monitoring plan to changing times.
Learn More Here
