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Sponsors: Are Your Sites Ready for an FDA Inspection?

Upcoming: February 29

Learn a comprehensive overview to prepare sponsors and sites for an FDA inspection.

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White Paper

GxP Compliance in Clinical Research

This white paper walks through key GxP principles and regulatory requirements and gives a real-world case study.

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Vendor Qualification vs Requalification Audits: What’s the Difference?

Audits to support your vendor qualification and management program should be conducted using a risk-based approach. Read more:

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4 min. read
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