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Good clinical practice (GCP) is an international quality standard, which governments can then transpose into regulations for clinical trials involving human subjects.

 
Blog

The Evolution of Clinical Quality: Key Considerations from ICH E6 R3

Explore the key updates in ICH E6 R3 and their impact on clinical quality

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3 min. read
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Webinar

Sponsors: Are Your Sites Ready for an FDA Inspection?

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

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E-Book

Making Good Clinical Practice More Understandable

This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.

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Webinar

Is Your Site Ready for an FDA Inspection?

Understand the FDA’s expectations for a site inspection, GCP compliance, and maintaining study integrity.

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Case Study

Advarra Consulting Delivers Clinical Trial Management Oversight

Download this case study to learn how Advarra Consulting mitigated risks and enabled compliance for a medical device organization.

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Blog

GCP Assessment During COVID – “Did Your Clinical Trials Remain GCP Compliant During COVID-19?”

Almost a year into the COVID-19 pandemic, analyze how IRB submissions, informed consent, and remote monitoring practices have maintained GCP compliance.

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5 min. read
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